Canonical Allele Identifier: PA2573073877
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_001362536.1:p.Trp506Cys
CA114387
NM_001375607.1:c.1518G>C
CA348406687
NM_001375607.1:c.1518G>T