Canonical Allele Identifier: PA2826362727
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 695489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Ala216Asp
CA1016036
NM_001253852.3:c.647C>A