Canonical Allele Identifier: PA2573274889
Gene: THAP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1552629
ClinVar RCV Id: RCV002197067 RCV003923497
ClinVar Variation Id: 1587439
ClinVar RCV Id: RCV002103288
ClinVar Variation Id: 2182219
ClinVar RCV Id: RCV002596060
ClinVar Variation Id: 2200643
ClinVar RCV Id: RCV002644187
ClinVar Variation Id: 2709573
ClinVar RCV Id: RCV003550033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065190.2:p.Gln130_Gln132del
CA8118233
NM_020457.3:c.388_396del