Canonical Allele Identifier: PA645499390
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420837
ClinVar RCV Id: RCV000481116 RCV001041709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu442Pro
CA16619115
NM_000051.4:c.1325T>C