Canonical Allele Identifier: PA916033828
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453616
ClinVar RCV Id: RCV000539253 RCV000560976 RCV003470677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln2066Glu
CA382550803
NM_001351834.2:c.6196C>G