Canonical Allele Identifier: PA916032243
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479088
ClinVar RCV Id: RCV000572582 RCV000699443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly844Ala
CA6265056
NM_001351834.2:c.2531G>C