Canonical Allele Identifier: PA2825033176
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 824785
ClinVar RCV Id: RCV001022279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1439Val
CA382531763
NM_000051.4:c.4315C>G