Canonical Allele Identifier: PA916032821
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186649
ClinVar RCV Id: RCV000166277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1258Gln
CA195438
NM_001351834.2:c.3774T>A
CA382524449
NM_001351834.2:c.3774T>G