Canonical Allele Identifier: PA916031346
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407585
ClinVar RCV Id: RCV000467265 RCV000579672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu176Val
CA6264627
NM_001351834.2:c.526C>G