Canonical Allele Identifier: PA2825034095
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1338011
ClinVar RCV Id: RCV001822609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile1849Thr
CA382545963
NM_000051.4:c.5546T>C