Canonical Allele Identifier: PA2826362681
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 859557
ClinVar RCV Id: RCV001065696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Arg113Gly
CA341689077
NM_001253852.3:c.337A>G