Canonical Allele Identifier: PA2825035096
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1003804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2293Pro
CA382556808
NM_000051.4:c.6878T>C