Canonical Allele Identifier: PA2826933324
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480026
ClinVar RCV Id: RCV001991146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Ala285Ser
CA341710434
NM_001308312.2:c.853G>T