Canonical Allele Identifier: PA2826866900
Gene: C12orf57 HGNC NCBI

Linked Data

ClinVar Variation Id: 41942
ClinVar RCV Id: RCV000034852 RCV000162118 RCV000254835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288763.1:p.Met1Val