Canonical Allele Identifier: PA165095
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn711Asp
CA165093
NM_000051.4:c.2131A>G