Canonical Allele Identifier: PA2826362813
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2179468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Gly444Asp
CA341710581
NM_001253852.3:c.1331G>A