Canonical Allele Identifier: PA658674168
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453434
ClinVar RCV Id: RCV000544792 RCV003470666 RCV004023637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser933Cys
CA228407758
NM_000051.4:c.2798C>G