Canonical Allele Identifier: PA916032948
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 629837
ClinVar RCV Id: RCV000774553 RCV001048918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser1362Gly
CA382528368
NM_001351834.2:c.4084A>G