Canonical Allele Identifier: PA2573203973
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1413110
ClinVar RCV Id: RCV001910299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly330Arg
CA382531228
NM_001351834.2:c.988G>A
CA382531229
NM_001351834.2:c.988G>C