Canonical Allele Identifier: PA2830003558
Gene: ACD HGNC NCBI

Linked Data

ClinVar Variation Id: 1167321
ClinVar RCV Id: RCV001516429 RCV001664943 RCV003487358
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Amino-acid Alleles

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