Canonical Allele Identifier: PA2825035093
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2761264
ClinVar RCV Id: RCV003500244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2292Leu
CA382556798
NM_000051.4:c.6875A>T