Canonical Allele Identifier: PA2825031920
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2774343
ClinVar RCV Id: RCV003585800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln876Leu
CA382544298
NM_000051.4:c.2627A>T