Canonical Allele Identifier: PA645503186
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236737
ClinVar RCV Id: RCV000228710 RCV001189492 RCV003318565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1802Arg
CA10582829
NM_000051.4:c.5405A>G