Canonical Allele Identifier: PA645377954
Gene: ACP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 374862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149059.1:p.Ser238Leu
CA9603108
NM_033068.3:c.713C>T