Canonical Allele Identifier: PA2825036491
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1373305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2897Cys
CA382523624
NM_000051.4:c.8689G>T