Canonical Allele Identifier: PA2825036000
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2691915
ClinVar RCV Id: RCV003494112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2701Met
CA6266274
NM_000051.4:c.8103A>G