Canonical Allele Identifier: PA2741866410
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2698425
ClinVar RCV Id: RCV003501029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu739Asp
CA382539099
NM_001351834.2:c.2217A>C
CA382539100
NM_001351834.2:c.2217A>T