Canonical Allele Identifier: PA157091
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133611
ClinVar RCV Id: RCV000120128 RCV000159703 RCV000528438 RCV000766496 RCV001355117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu958Gly
CA157089
NM_000051.4:c.2873A>G