Canonical Allele Identifier: PA916033460
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825668
ClinVar RCV Id: RCV001023955 RCV001862277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1782Glu
CA382543176
NM_001351834.2:c.5344A>G