Canonical Allele Identifier: PA645413873
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 381581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Ser266Ala
CA16606005
NM_001040716.2:c.796T>G