Canonical Allele Identifier: PA2825032282
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2195814
ClinVar RCV Id: RCV002628964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Tyr1034Cys
CA382515107
NM_000051.4:c.3101A>G