Canonical Allele Identifier: PA091811
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3023
ClinVar RCV Id: RCV000003160 RCV000003161 RCV000003159 RCV000115244 RCV000168223 RCV000212060 RCV000417259 RCV000515429 RCV000709707 RCV003149562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2424Gly
CA115930
NM_000051.4:c.7271T>G