Canonical Allele Identifier: PA2826933321
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469161
ClinVar RCV Id: RCV001972955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Glu280Lys
CA341710536
NM_001308312.2:c.838G>A