Canonical Allele Identifier: PA2499250955
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1171142
ClinVar RCV Id: RCV001524063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His636Pro
CA382536305
NM_001351834.2:c.1907A>C