Canonical Allele Identifier: PA2830100621
Gene: ABHD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3130399
ClinVar RCV Id: RCV004420814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116248.2:p.Pro32Leu
CA388628647
NM_032859.3:c.95C>T