Canonical Allele Identifier: PA2825035812
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2756015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2617Gly
CA382561369
NM_000051.4:c.7850T>G