Canonical Allele Identifier: PA916032566
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 422903
ClinVar RCV Id: RCV000481827 RCV000556279 RCV000574851 RCV002271512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Trp1058Cys
CA16619156
NM_001351834.2:c.3174G>C
CA382515596
NM_001351834.2:c.3174G>T