Canonical Allele Identifier: PA091796
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu1465Pro
CA298357
NM_000051.4:c.4394T>C