Canonical Allele Identifier: PA891845032
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 571794
ClinVar RCV Id: RCV000693030 RCV000771456 RCV001571988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn914Ser
CA6265105
NM_000051.4:c.2741A>G