Canonical Allele Identifier: PA2825035125
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2054375
ClinVar RCV Id: RCV002909767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2304Gly
CA382557025
NM_000051.4:c.6911A>G