Canonical Allele Identifier: PA916032982
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453506
ClinVar RCV Id: RCV000531934 RCV000777907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asn1395Ser
CA228374758
NM_001351834.2:c.4184A>G