Canonical Allele Identifier: PA2825035926
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1761651
ClinVar RCV Id: RCV002419224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2670Asn
CA382561819
NM_000051.4:c.8010G>C
CA382561820
NM_000051.4:c.8010G>T