Canonical Allele Identifier: PA2825219922
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Thr568Ala
CA6131288
NM_000920.4:c.1702A>G