Canonical Allele Identifier: PA645498706
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu240Arg
CA10578973
NM_000051.4:c.719T>G