Canonical Allele Identifier: PA658669577
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 485220
ClinVar RCV Id: RCV000561120 RCV001526805 RCV001764680 RCV003465256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1848Gly
CA382545940
NM_000051.4:c.5543A>G