Canonical Allele Identifier: PA2825034068
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1718388
ClinVar RCV Id: RCV002304889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys1838Ser
CA382545743
NM_000051.4:c.5512T>A
CA382545754
NM_000051.4:c.5513G>C