Canonical Allele Identifier: PA658670110
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478983
ClinVar RCV Id: RCV000561076 RCV000628114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2317Thr
CA6266036
NM_000051.4:c.6950A>C