Canonical Allele Identifier: PA645413937
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Ala1114Val
CA6130812
NM_001040716.2:c.3341C>T