Allele Registry

Canonical Allele Identifier: PA2830003558

Gene: ACD HGNC NCBI

ClinVar RCV:

RCV001516429

RCV001664943

RCV003487358

ClinVar Variation:

1167321

HGVS (amino-acid)	Matching Registered Transcripts
NP_075065.3:p.Val429Ala	CA8114380 NM_022914.3:c.1286T>C