Canonical Allele Identifier: PA2825031902
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1391357
ClinVar RCV Id: RCV001893035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn870Ser
CA382544153
NM_000051.4:c.2609A>G