Canonical Allele Identifier: PA2825030654
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2747314
ClinVar RCV Id: RCV003501957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu318Arg
CA382530904
NM_000051.4:c.953T>G