Canonical Allele Identifier: PA658670779
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481180
ClinVar RCV Id: RCV000569218 RCV001220325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2756Arg
CA382562700
NM_000051.4:c.8267A>G