Canonical Allele Identifier: PA111592
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Arg272Cys
CA114414
NM_000312.4:c.814C>T