Canonical Allele Identifier: PA2825034267
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1061765
ClinVar RCV Id: RCV001371408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala1931Thr
CA382548330
NM_000051.4:c.5791G>A