Canonical Allele Identifier: PA915969886
Gene: ACD HGNC NCBI

Linked Data

ClinVar Variation Id: 542421
ClinVar RCV Id: RCV000652840 RCV001816641 RCV003237977 RCV003953202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001075955.2:p.Thr205Ala
CA8114609
NM_001082486.2:c.613A>G