Canonical Allele Identifier: PA2825030637
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1039826
ClinVar RCV Id: RCV001343376 RCV002377455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile311Thr
CA382530706
NM_000051.4:c.932T>C