Canonical Allele Identifier: PA2825030684
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1413110
ClinVar RCV Id: RCV001910299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly330Arg
CA382531228
NM_000051.4:c.988G>A
CA382531229
NM_000051.4:c.988G>C