Canonical Allele Identifier: PA287011
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 127455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Val2705Leu
CA287009
NM_000051.4:c.8113G>T
CA382562143
NM_000051.4:c.8113G>C