Canonical Allele Identifier: PA916031355
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 132685
ClinVar RCV Id: RCV000119106 RCV000120166 RCV000131001 RCV000223988 RCV002225343 RCV001354360 RCV003315697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val182Leu
CA157195
NM_001351834.2:c.544G>C