Canonical Allele Identifier: PA916021050
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 390620
ClinVar RCV Id: RCV000436086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Ala48Gly
CA16603384
NM_001308312.2:c.143C>G