Canonical Allele Identifier: PA645501048
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 246009
ClinVar RCV Id: RCV000236403 RCV003165661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu848Lys
CA10584332
NM_000051.4:c.2542G>A