Canonical Allele Identifier: PA916033671
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127413
ClinVar RCV Id: RCV000115218 RCV000195828 RCV000763707 RCV000589184 RCV001799619 RCV001263508 RCV003237337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr1961Cys
CA286907
NM_001351834.2:c.5882A>G