Canonical Allele Identifier: PA2825036184
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 956933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2774Ala
CA228364814
NM_000051.4:c.8321T>C