Canonical Allele Identifier: PA2741866909
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2707210
ClinVar RCV Id: RCV003501235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1441Arg
CA382531838
NM_001351834.2:c.4322T>G