Canonical Allele Identifier: PA658670741
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2725Gly
CA382562502
NM_000051.4:c.8174A>G