Canonical Allele Identifier: PA916035125
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181908
ClinVar RCV Id: RCV000159672 RCV000200661 RCV000589071 RCV003467224 RCV004551370
ClinVar Variation Id: 2100366
ClinVar RCV Id: RCV003025873 RCV004068588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val3056Leu
CA298108
NM_001351834.2:c.9166G>T
CA382532204
NM_001351834.2:c.9166G>C