Canonical Allele Identifier: PA2825035805
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2040053
ClinVar RCV Id: RCV002886223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg2613Ser
CA382561343
NM_000051.4:c.7839A>C
CA382561344
NM_000051.4:c.7839A>T