Canonical Allele Identifier: PA2828305538
Gene: AP1S2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2218349
ClinVar RCV Id: RCV002687209 RCV003435890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355937.1:p.Val38Ile
CA10356469
NM_001369008.1:c.112G>A