Canonical Allele Identifier: PA645503640
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2076Val
CA6265897
NM_000051.4:c.6226A>G