Canonical Allele Identifier: PA658817381
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 520727
ClinVar RCV Id: RCV000623523 RCV001849410 RCV002531883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Arg206Gln
CA1016061
NM_006594.5:c.617G>A