Canonical Allele Identifier: PA891845261
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 572731
ClinVar RCV Id: RCV000694183 RCV002343482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe1869Val
CA382546254
NM_000051.4:c.5605T>G