Canonical Allele Identifier: PA2828620812
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 657
ClinVar RCV Id: RCV000000691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362532.1:p.Trp499Cys
CA114387
NM_001375603.1:c.1497G>C
CA348406687
NM_001375603.1:c.1497G>T