Allele Registry

Canonical Allele Identifier: PA2830003580

Gene: ACD HGNC NCBI

ClinVar RCV:

RCV003172551

ClinVar Variation:

2452457

HGVS (amino-acid)	Matching Registered Transcripts
NP_075065.3:p.Gln434Arg	CA396349718 NM_022914.3:c.1301A>G