Canonical Allele Identifier: PA916034605
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490724
ClinVar RCV Id: RCV000582097 RCV000706251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Phe2686Leu
CA382561941
NM_001351834.2:c.8056T>C
CA382561951
NM_001351834.2:c.8058T>A
CA382561952
NM_001351834.2:c.8058T>G