Canonical Allele Identifier: PA916034612
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478934
ClinVar RCV Id: RCV000823662 RCV000561362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2694Arg
CA382562025
NM_001351834.2:c.8080G>A
CA382562026
NM_001351834.2:c.8080G>C