Canonical Allele Identifier: PA2825031858
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1034587
ClinVar RCV Id: RCV001337330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln852Arg
CA382543761
NM_000051.4:c.2555A>G