Canonical Allele Identifier: PA916033492
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 230134
ClinVar RCV Id: RCV000222750 RCV000674622 RCV001030596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala1812Val
CA10579181
NM_001351834.2:c.5435C>T