Canonical Allele Identifier: PA916034049
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481117
ClinVar RCV Id: RCV000569640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2245Gly
CA382555154
NM_001351834.2:c.6734A>G