Canonical Allele Identifier: PA645377929
Gene: ACP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 374864
ClinVar RCV Id: RCV000415588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149059.1:p.Arg76Cys
CA16043945
NM_033068.3:c.226C>T