Canonical Allele Identifier: PA916032966
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233567
ClinVar RCV Id: RCV000217705 RCV000779766 RCV000805982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1382Leu
CA6265409
NM_001351834.2:c.4145C>T