Canonical Allele Identifier: PA2825030447
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 660381
ClinVar RCV Id: RCV000817562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Leu233Phe
CA382529115
NM_000051.4:c.699A>C
CA382529119
NM_000051.4:c.699A>T