Canonical Allele Identifier: PA2573083349
Gene: AP1S2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302899
ClinVar RCV Id: RCV001756398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003907.3:p.Leu15Arg
CA412459498
NM_003916.5:c.44T>G