Canonical Allele Identifier: PA916065379
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071504.2:p.Ala573Thr
CA312896
NM_022172.3:c.1717G>A