Canonical Allele Identifier: PA891850566
Gene: ACP5 HGNC NCBI

Linked Data

ClinVar Variation Id: 582172
ClinVar RCV Id: RCV000706171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001602.1:p.Thr157Ala
CA404146959
NM_001611.5:c.469A>G