Canonical Allele Identifier: PA2825030665
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1488377
ClinVar RCV Id: RCV001988549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile323Lys
CA382531026
NM_000051.4:c.968T>A