Canonical Allele Identifier: PA916031713
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 560752
ClinVar RCV Id: RCV000679098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu435Ser
CA382533611
NM_001351834.2:c.1304T>C