Canonical Allele Identifier: PA2825032288
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1348757
ClinVar RCV Id: RCV002035034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser1037Pro
CA382515156
NM_000051.4:c.3109T>C