Canonical Allele Identifier: PA2825032978
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1338Gly
CA228371374
NM_000051.4:c.4012A>G