Canonical Allele Identifier: PA198314
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2622Gly
CA198312
NM_000051.4:c.7865C>G