Canonical Allele Identifier: PA2573262691
Gene: ABHD12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497185
ClinVar RCV Id: RCV001992262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056415.1:p.Ser21Phe
CA9796328
NM_015600.5:c.62C>T