Canonical Allele Identifier: PA2825031442
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1001572
ClinVar RCV Id: RCV001297891 RCV002418896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp661His
CA382536884
NM_000051.4:c.1981G>C