Canonical Allele Identifier: PA916031852
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 819723
ClinVar RCV Id: RCV001012524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr547Ala
CA382534528
NM_001351834.2:c.1639A>G