Canonical Allele Identifier: PA1139733984
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 927891
ClinVar RCV Id: RCV001191463 RCV001219750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile559Met
CA382535142
NM_001351834.2:c.1677A>G