Canonical Allele Identifier: PA2825034081
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1502681
ClinVar RCV Id: RCV002011051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr1844Ser
CA382545871
NM_000051.4:c.5531A>C