Canonical Allele Identifier: PA916031970
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 820333
ClinVar RCV Id: RCV001013685 RCV001175461 RCV001242715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp639His
CA382536400
NM_001351834.2:c.1915G>C