Canonical Allele Identifier: PA2825033956
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1746959
ClinVar RCV Id: RCV002346919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu1783Gln
CA382543209
NM_000051.4:c.5347G>C