Canonical Allele Identifier: PA2825031606
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2086236
ClinVar RCV Id: RCV003007387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala736Gly
CA382539025
NM_000051.4:c.2207C>G