Canonical Allele Identifier: PA916035241
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 660737
ClinVar RCV Id: RCV000817994 RCV001176201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338765.1:p.Arg76Ser
CA382521446
NM_001351836.2:c.228A>T
CA382521449
NM_001351836.2:c.228A>C