Allele Registry

Canonical Allele Identifier: PA2830003544

Gene: ACD HGNC NCBI

ClinVar RCV:

RCV001984962

RCV002397962

ClinVar Variation:

1435630

HGVS (amino-acid)	Matching Registered Transcripts
NP_075065.3:p.Arg425Trp	CA8114381 NM_022914.3:c.1273C>T