Canonical Allele Identifier: PA2826362747
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2041494
ClinVar RCV Id: RCV002891136 RCV003375709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Leu274Phe
CA1016005
NM_001253852.3:c.820C>T