Canonical Allele Identifier: PA2825035098
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1755907
ClinVar RCV Id: RCV002362207 RCV003776319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2293Gln
CA382556805
NM_000051.4:c.6878T>A