Canonical Allele Identifier: PA916034035
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826555
ClinVar RCV Id: RCV001025540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2232Asp
CA382554915
NM_001351834.2:c.6696G>C
CA382554916
NM_001351834.2:c.6696G>T