Canonical Allele Identifier: PA2828620449
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362531.1:p.Gly404Ser
CA114399
NM_001375602.1:c.1210G>A