Canonical Allele Identifier: PA2825031465
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 846132
ClinVar Variation Id: 1486360

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His674Gln
CA382537351
NM_000051.4:c.2022C>G
CA382537352
NM_000051.4:c.2022C>A