Canonical Allele Identifier: PA2825031881
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1793422
ClinVar RCV Id: RCV002426088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Pro862Arg
CA382543981
NM_000051.4:c.2585C>G