Canonical Allele Identifier: PA2573204731
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1503093
ClinVar RCV Id: RCV002045343 RCV003303619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly880Arg
CA382544367
NM_001351834.2:c.2638G>C