Canonical Allele Identifier: PA2825034448
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2820569
ClinVar RCV Id: RCV003606293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser2017_Leu2018insPhe
CA2739265975
NM_000051.4:c.6051_6053dup