Canonical Allele Identifier: PA645500635
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407691
ClinVar RCV Id: RCV000476884 RCV000775701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu688Gln
CA16613357
NM_000051.4:c.2062G>C