Canonical Allele Identifier: PA2825034439
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 944000
ClinVar Variation Id: 3222152
ClinVar RCV Id: RCV004513570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2013Arg
CA382549906
NM_000051.4:c.6037G>A
CA382549907
NM_000051.4:c.6037G>C