Canonical Allele Identifier: PA2825035840
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2162281
ClinVar RCV Id: RCV003091199 RCV003994496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr2627Ser
CA382561431
NM_000051.4:c.7880A>C