Allele Registry

Canonical Allele Identifier: PA2580489740

Gene: ACMSD HGNC NCBI

ClinVar Allele:

2223061

ClinVar RCV:

RCV004103640

ClinVar Variation:

2242705

HGVS (amino-acid)	Matching Registered Transcripts
NP_612199.2:p.Trp26Arg	CA348647649 NM_138326.3:c.76T>A CA348647650 NM_138326.3:c.76T>C