Canonical Allele Identifier: PA658673594
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453348
ClinVar RCV Id: RCV000551994 RCV003584639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Phe336Cys
CA228386405
NM_000051.4:c.1007T>G