Canonical Allele Identifier: PA312898
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Ala573Thr
CA312896
NM_001040716.2:c.1717G>A