Canonical Allele Identifier: PA916031422
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142522
ClinVar RCV Id: RCV000131698 RCV000205199 RCV000211951 RCV000587384 RCV001257492 RCV004551265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys224Glu
CA294425
NM_001351834.2:c.670A>G