Canonical Allele Identifier: PA2825031794
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 864006
ClinVar RCV Id: RCV001071096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe825Val
CA382543127
NM_000051.4:c.2473T>G