Canonical Allele Identifier: PA2826362676
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310614
ClinVar RCV Id: RCV001767728
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Arg107Gly
CA1016139
NM_001253852.3:c.319C>G