Canonical Allele Identifier: PA2826362730
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210196
ClinVar RCV Id: RCV000193319 RCV001852544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Arg224Cys
CA206714
NM_001253852.3:c.670C>T