Canonical Allele Identifier: PA916032216
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407579
ClinVar RCV Id: RCV000572358 RCV000679103 RCV000466846 RCV002298598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg832Leu
CA6265050
NM_001351834.2:c.2495G>T