Canonical Allele Identifier: PA2826933317
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2179468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Gly276Asp
CA341710581
NM_001308312.2:c.827G>A