Canonical Allele Identifier: PA2828621099
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 676
ClinVar RCV Id: RCV000000711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362533.1:p.Ile466Met
CA114422
NM_001375604.1:c.1398C>G