Canonical Allele Identifier: PA645413904
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Thr568Ala
CA6131288
NM_001040716.2:c.1702A>G