Canonical Allele Identifier: PA2825031925
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1023332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser877Gly
CA382544318
NM_000051.4:c.2629A>G