Canonical Allele Identifier: PA2741866521
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2709332
ClinVar RCV Id: RCV003501282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu885Val
CA382545032
NM_001351834.2:c.2653T>G