Canonical Allele Identifier: PA916032214
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 140867
ClinVar RCV Id: RCV000129082 RCV000199664 RCV000211982 RCV000587618 RCV003492583 RCV004551237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg832Cys
CA293954
NM_001351834.2:c.2494C>T