Canonical Allele Identifier: PA2826362724
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 520727
ClinVar RCV Id: RCV000623523 RCV001849410 RCV002531883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Arg206Gln
CA1016061
NM_001253852.3:c.617G>A