Canonical Allele Identifier: PA2825034002
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1747392
ClinVar RCV Id: RCV002349444 RCV003102728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1806Val
CA382543864
NM_000051.4:c.5416A>G