Canonical Allele Identifier: PA2825035967
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1426261
ClinVar RCV Id: RCV001929322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2691Leu
CA382562003
NM_000051.4:c.8072G>T