Canonical Allele Identifier: PA2825035513
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 665454
ClinVar RCV Id: RCV000823743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2471Ser
CA382560163
NM_000051.4:c.7412T>G