Canonical Allele Identifier: PA2825219222
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 381581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Ser266Ala
CA16606005
NM_000920.4:c.796T>G