Canonical Allele Identifier: PA2825030611
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1005823
ClinVar RCV Id: RCV001302768 RCV002375368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly301Arg
CA382529658
NM_000051.4:c.901G>C