Canonical Allele Identifier: PA916033933
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 231452
ClinVar RCV Id: RCV000213307 RCV000791592 RCV002225521 RCV003462463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg2138Gly
CA6265932
NM_001351834.2:c.6412A>G