Canonical Allele Identifier: PA286939
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127425
ClinVar RCV Id: RCV000115230 RCV000196735 RCV000212044 RCV000587205 RCV002225324 RCV004549564 RCV003492464
ClinVar Variation Id: 1692881
ClinVar RCV Id: RCV002259276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2181Asp
CA286937
NM_000051.4:c.6543G>T
CA382554300
NM_000051.4:c.6543G>C