Canonical Allele Identifier: PA2741866512
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2698356
ClinVar RCV Id: RCV003501027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln876Glu
CA382544288
NM_001351834.2:c.2626C>G