Canonical Allele Identifier: PA645507280
Gene: THAP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 393304
ClinVar RCV Id: RCV000498990 RCV002522728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065190.2:p.Phe80Leu
CA396396079
NM_020457.3:c.238T>C
CA396396087
NM_020457.3:c.240C>A
CA396396088
NM_020457.3:c.240C>G