Canonical Allele Identifier: PA645503723
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231111
ClinVar RCV Id: RCV000215989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2255Arg
CA10579234
NM_000051.4:c.6764T>G