Canonical Allele Identifier: PA2826362736
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393895
ClinVar RCV Id: RCV001898397 RCV004041499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Gly250Asp
CA1016019
NM_001253852.3:c.749G>A