Canonical Allele Identifier: PA2825035872
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2995033
ClinVar RCV Id: RCV003850640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2647Val
CA382561674
NM_000051.4:c.7939A>G