Canonical Allele Identifier: PA916032783
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142043
ClinVar RCV Id: RCV000130847 RCV000200096 RCV000587182 RCV001357259 RCV003321515 RCV003474771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1230Ser
CA294243
NM_001351834.2:c.3689A>G