Canonical Allele Identifier: PA2573262889
Gene: ABHD12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1357190
ClinVar RCV Id: RCV001878236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056415.1:p.Thr276Ile
CA408455883
NM_015600.5:c.827C>T