Canonical Allele Identifier: PA658673569
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453765
ClinVar RCV Id: RCV000547848 RCV000575483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr306Ala
CA382530530
NM_000051.4:c.916A>G