Canonical Allele Identifier: PA916034225
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186868
ClinVar RCV Id: RCV000166522 RCV000168469 RCV000590313 RCV000855629 RCV001356845 RCV003468786 RCV003483546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2392Trp
CA196089
NM_001351834.2:c.7174C>T