Allele Registry

Canonical Allele Identifier: PA312932

Gene: PC HGNC NCBI

ClinVar Allele:

200189

ClinVar RCV:

RCV000186130

RCV000675135

ClinVar Variation:

203924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035806.1:p.Thr908Met	CA312930 NM_001040716.2:c.2723C>T