Canonical Allele Identifier: PA2826933315
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2554151
ClinVar RCV Id: RCV003304086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Ile272Leu
CA28995389
NM_001308312.2:c.814A>C