Canonical Allele Identifier: PA916032022
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232113
ClinVar RCV Id: RCV000215407 RCV000467380 RCV000763689 RCV003231407 RCV001778808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly679Val
CA6264919
NM_001351834.2:c.2036G>T