Allele Registry

Canonical Allele Identifier: PA2573177391

Gene: ACD HGNC NCBI

ClinVar RCV:

RCV001984962

RCV002397962

ClinVar Variation:

1435630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075955.2:p.Arg428Trp	CA8114381 NM_001082486.2:c.1282C>T