Canonical Allele Identifier: PA2825589533
Gene: AP1G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2465492
ClinVar RCV Id: RCV003185625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119.3:p.Pro471Ala
CA8156100
NM_001128.6:c.1411C>G