Canonical Allele Identifier: PA2825560304
Gene: ACP5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349238
ClinVar RCV Id: RCV002035159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104505.1:p.Phe167Ser
CA404146858
NM_001111035.3:c.500T>C