Canonical Allele Identifier: PA2829671071
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2623900
ClinVar RCV Id: RCV003377325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Ser242Arg
CA341713739
NM_006594.5:c.726T>G
CA341713741
NM_006594.5:c.726T>A
CA341713748
NM_006594.5:c.724A>C