Canonical Allele Identifier: PA916032070
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453404
ClinVar RCV Id: RCV000539773 RCV000579664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu715Pro
CA382538710
NM_001351834.2:c.2144T>C