Canonical Allele Identifier: PA2825031459
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1463259
ClinVar RCV Id: RCV001960958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly670Val
CA382537072
NM_000051.4:c.2009G>T