Canonical Allele Identifier: PA658673908
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453401
ClinVar RCV Id: RCV000549814 RCV001014244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn685Ser
CA382537462
NM_000051.4:c.2054A>G