Canonical Allele Identifier: PA2830003566
Gene: ACD HGNC NCBI

Linked Data

ClinVar Variation Id: 1775181
ClinVar RCV Id: RCV002405334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075065.3:p.Arg430Ser
CA396349743
NM_022914.3:c.1290G>C
CA396349746
NM_022914.3:c.1290G>T