Canonical Allele Identifier: PA2573202199
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1448889
ClinVar RCV Id: RCV001997279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1360Arg
CA382528275
NM_001351834.2:c.4078A>C
CA382528311
NM_001351834.2:c.4080T>A
CA382528312
NM_001351834.2:c.4080T>G