Canonical Allele Identifier: PA2828621598
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362535.1:p.Gly399Ser
CA114399
NM_001375606.1:c.1195G>A