Canonical Allele Identifier: PA916033030
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 824785
ClinVar RCV Id: RCV001022279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1439Val
CA382531763
NM_001351834.2:c.4315C>G