Canonical Allele Identifier: PA2825031441
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1037709
ClinVar RCV Id: RCV001340902
ClinVar Variation Id: 1783809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met660Ile
CA382536872
NM_000051.4:c.1980G>A
CA382536874
NM_000051.4:c.1980G>C
CA382536878
NM_000051.4:c.1980G>T