Canonical Allele Identifier: PA2573203801
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1386065
ClinVar RCV Id: RCV001889148 RCV003229064 RCV003166931 RCV003464205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2253Glu
CA382555308
NM_001351834.2:c.6757A>G