Allele Registry

Canonical Allele Identifier: PA312898

Gene: PC HGNC NCBI

ClinVar Allele:

200198

ClinVar RCV:

RCV000186118

RCV001824667

RCV003323437

ClinVar Variation:

203912

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