Canonical Allele Identifier: PA2825589513
Gene: AP1G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119.3:p.Met366Val
CA8156200
NM_001128.6:c.1096A>G