Canonical Allele Identifier: PA645500537
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232506
ClinVar RCV Id: RCV000217508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu668Lys
CA10579036
NM_000051.4:c.2002G>A