Canonical Allele Identifier: PA645504166
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 234050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2644Ser
CA10579276
NM_000051.4:c.7930G>A