Canonical Allele Identifier: PA2826363044
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469161
ClinVar RCV Id: RCV001972955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Glu349Lys
CA341710536
NM_001253853.3:c.1045G>A