Canonical Allele Identifier: PA211734
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 161342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Arg189Trp
CA211732
NM_000312.4:c.565C>T