Canonical Allele Identifier: PA173989
Gene: AP1S3 HGNC NCBI

Linked Data

ClinVar Variation Id: 160375
ClinVar RCV Id: RCV000148042 RCV000454575 RCV002262754 RCV003927448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034658.1:p.Arg33Trp
CA173988
NM_001039569.2:c.97C>T