Canonical Allele Identifier: PA658673499
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His231Asp
CA382529076
NM_000051.4:c.691C>G