Canonical Allele Identifier: PA2741867377
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2715586
ClinVar RCV Id: RCV003501384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2123Arg
CA382553219
NM_001351834.2:c.6367A>C
CA382553230
NM_001351834.2:c.6369T>A
CA382553233
NM_001351834.2:c.6369T>G