Allele Registry

Canonical Allele Identifier: PA111797

Gene: PC HGNC NCBI

ClinVar RCV:

RCV000020384

RCV000484861

ClinVar Variation:

21222

HGVS (amino-acid)	Matching Registered Transcripts
NP_000911.2:p.Arg631Gln	CA341754 NM_000920.4:c.1892G>A