Canonical Allele Identifier: PA2825031415
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2774199
ClinVar RCV Id: RCV003585787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val648Gly
CA382536644
NM_000051.4:c.1943T>G