Canonical Allele Identifier: PA916031379
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420008
ClinVar RCV Id: RCV000482564 RCV000569534 RCV000806962 RCV003470549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly197Glu
CA6264634
NM_001351834.2:c.590G>A