Allele Registry

Canonical Allele Identifier: PA2828621869

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV002223411

ClinVar Variation:

1677377

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362537.1:p.Phe162Leu	CA348400954 NM_001375608.1:c.484T>C CA348400967 NM_001375608.1:c.486C>A CA348400969 NM_001375608.1:c.486C>G