Canonical Allele Identifier: PA2828620898
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362533.1:p.His170Pro
CA114428
NM_001375604.1:c.509A>C