Canonical Allele Identifier: PA312897
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 203912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Ala573Thr
CA312896
NM_000920.4:c.1717G>A