Canonical Allele Identifier: PA916033902
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482630
ClinVar RCV Id: RCV000574099 RCV001350510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2110Glu
CA6265904
NM_001351834.2:c.6330C>G
CA382552262
NM_001351834.2:c.6330C>A