Canonical Allele Identifier: PA2825035095
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1755904
ClinVar RCV Id: RCV002362205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2293Val
CA6266025
NM_000051.4:c.6877C>G