Allele Registry

Canonical Allele Identifier: PA2829079337

Gene: ACSL5 HGNC NCBI

ClinVar RCV:

RCV004097805

ClinVar Variation:

2233770

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373966.1:p.Ile594Thr	CA378411014 NM_001387037.1:c.1781T>C