Canonical Allele Identifier: PA2573071108
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1313661
ClinVar RCV Id: RCV001764025 RCV002324187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly1102Glu
CA382517364
NM_001351834.2:c.3305G>A