Canonical Allele Identifier: PA2825035090
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1171795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Trp2291Cys
CA382556785
NM_000051.4:c.6873G>C
CA382556786
NM_000051.4:c.6873G>T