Canonical Allele Identifier: PA2828622049
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 676
ClinVar RCV Id: RCV000000711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362537.1:p.Ile426Met
CA114422
NM_001375608.1:c.1278C>G