Canonical Allele Identifier: PA335770
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 216851
ClinVar RCV Id: RCV000195567 RCV001015890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ser865del
CA335768
NM_000051.4:c.2593_2595del