Canonical Allele Identifier: PA2825033994
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922886
ClinVar RCV Id: RCV001183193 RCV001341538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1802Tyr
CA382543764
NM_000051.4:c.5404C>T