Canonical Allele Identifier: PA169890
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142966
ClinVar RCV Id: RCV000132462 RCV000168295 RCV000236226 RCV001201309 RCV001355859 RCV002225449 RCV001798460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met963Val
CA169888
NM_000051.4:c.2887A>G