Canonical Allele Identifier: PA916033799
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 826204
ClinVar RCV Id: RCV001024940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Tyr2049Lys
CA915947653
NM_001351834.2:c.6145_6147delinsAAA