Canonical Allele Identifier: PA916034593
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3045
ClinVar RCV Id: RCV000003186 RCV000545206 RCV001027090 RCV004018544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2677Cys
CA249431
NM_001351834.2:c.8030A>G