Canonical Allele Identifier: PA2580139807
Gene: AP1G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1708218
ClinVar RCV Id: RCV002287591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119.3:p.Arg15Trp
CA396673846
NM_001128.6:c.43C>T