Canonical Allele Identifier: PA2825030692
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 644228
ClinVar RCV Id: RCV000798104 RCV002386409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr332Cys
CA6264716
NM_000051.4:c.995A>G