Canonical Allele Identifier: PA916032778
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453482
ClinVar RCV Id: RCV000531288 RCV002456026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp1226Gly
CA382523290
NM_001351834.2:c.3677A>G