Canonical Allele Identifier: PA2825589499
Gene: AP1G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3127438
ClinVar RCV Id: RCV004424791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119.3:p.Pro206Ala
CA8156462
NM_001128.6:c.616C>G