Canonical Allele Identifier: PA658670059
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481117
ClinVar RCV Id: RCV000569640
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu2245Gly
CA382555154
NM_000051.4:c.6734A>G