Canonical Allele Identifier: PA157167
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 133631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu2332Pro
CA157165
NM_000051.4:c.6995T>C