Canonical Allele Identifier: PA174624
Gene: ARPP21 HGNC NCBI

Linked Data

ClinVar Variation Id: 161701
ClinVar RCV Id: RCV000149237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057384.2:p.Gly452Val
CA174623
NM_016300.4:c.1355G>T