Canonical Allele Identifier: PA298353
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181994
ClinVar RCV Id: RCV000159763 RCV000474326 RCV001290629 RCV002466454 RCV003225035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1283Pro
CA298351
NM_000051.4:c.3848T>C