Canonical Allele Identifier: PA312917
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Val166Ile
CA312915
NM_001040716.2:c.496G>A