Canonical Allele Identifier: PA2829715775
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3122451
ClinVar RCV Id: RCV004413856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037407.4:p.Pro1933Leu
CA8241717
NM_013275.6:c.5798C>T