Canonical Allele Identifier: PA2828620365
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362531.1:p.Arg281Trp
CA114410
NM_001375602.1:c.841C>T