Canonical Allele Identifier: PA2825036072
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1509331
ClinVar RCV Id: RCV002040647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp2725Tyr
CA382562500
NM_000051.4:c.8173G>T