Canonical Allele Identifier: PA658674304
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481334
ClinVar RCV Id: RCV000566290 RCV001858173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln1098Glu
CA382517285
NM_000051.4:c.3292C>G