Canonical Allele Identifier: PA2825030091
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1782491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu64Val
CA382521108
NM_000051.4:c.190T>G