Canonical Allele Identifier: PA2828623036
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362542.1:p.Gln226His
CA114416
NM_001375613.1:c.678G>C
CA348401830
NM_001375613.1:c.678G>T