Canonical Allele Identifier: PA2825034264
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 926004
ClinVar RCV Id: RCV001188287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1930Gly
CA382548327
NM_000051.4:c.5789A>G