Canonical Allele Identifier: PA916069090
Gene: ACD HGNC NCBI

Linked Data

ClinVar Variation Id: 434071
ClinVar RCV Id: RCV000503600 RCV000694462 RCV001702497 RCV003243155 RCV003962366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075065.3:p.Val8Ile
CA8114847
NM_022914.3:c.22G>A