Canonical Allele Identifier: PA355742
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 219594
ClinVar RCV Id: RCV000205336 RCV000222128 RCV001193061 RCV001356715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr2666Ala
CA349494
NM_000051.4:c.7996A>G