Canonical Allele Identifier: PA2741852556
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2623900
ClinVar RCV Id: RCV003377325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Ser74Arg
CA341713739
NM_001308312.2:c.222T>G
CA341713741
NM_001308312.2:c.222T>A
CA341713748
NM_001308312.2:c.220A>C