Canonical Allele Identifier: PA2580203315
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1719759
ClinVar RCV Id: RCV002305019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val682Gly
CA382537431
NM_001351834.2:c.2045T>G