Canonical Allele Identifier: PA2826362675
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 828196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Arg107Trp
CA1016140
NM_001253852.3:c.319C>T