Canonical Allele Identifier: PA2827629543
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3223196
ClinVar RCV Id: RCV004508551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2716del
CA2825001960
NM_001351834.2:c.8146_8148del