Canonical Allele Identifier: PA916033525
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1846Val
CA286897
NM_001351834.2:c.5536A>G