Canonical Allele Identifier: PA2825030617
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2005973
ClinVar RCV Id: RCV002837565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr303Cys
CA382530443
NM_000051.4:c.908A>G