Canonical Allele Identifier: PA645504159
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Trp2638Cys
CA6266211
NM_000051.4:c.7914G>T
CA382561504
NM_000051.4:c.7914G>C