Canonical Allele Identifier: PA2825034435
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1361918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2009Cys
CA382549868
NM_000051.4:c.6026A>G