Canonical Allele Identifier: PA916031387
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407497
ClinVar RCV Id: RCV000470467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser200Cys
CA16613053
NM_001351834.2:c.599C>G