Canonical Allele Identifier: PA2825404149
Gene: ABHD12 HGNC NCBI

Linked Data

ClinVar Variation Id: 337997
ClinVar RCV Id: RCV000362453 RCV000997762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035937.1:p.Val68Ala
CA9796219
NM_001042472.3:c.203T>C