Canonical Allele Identifier: PA2573197979
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393895
ClinVar RCV Id: RCV001898397 RCV004041499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Gly82Asp
CA1016019
NM_001308312.2:c.245G>A