Canonical Allele Identifier: PA916032269
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 478965
ClinVar RCV Id: RCV000575368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser854Cys
CA382543802
NM_001351834.2:c.2561C>G