Canonical Allele Identifier: PA645426138
Gene: AP4E1 HGNC NCBI

Linked Data

ClinVar Variation Id: 240837
ClinVar RCV Id: RCV000232082 RCV002293430 RCV003987469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031373.2:p.Val618Ile
CA7559184
NM_007347.5:c.1852G>A