Canonical Allele Identifier: PA2825034214
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1036842
ClinVar RCV Id: RCV001339903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg1907Gly
CA382547927
NM_000051.4:c.5719A>G