Canonical Allele Identifier: PA2825035982
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 636708
ClinVar RCV Id: RCV000788614 RCV000792375
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly2695Ala
CA382562039
NM_000051.4:c.8084G>C