Canonical Allele Identifier: PA2825404282
Gene: ABHD12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357190
ClinVar RCV Id: RCV001878236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035937.1:p.Thr276Ile
CA408455883
NM_001042472.3:c.827C>T