Canonical Allele Identifier: PA2825031392
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 820333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp639His
CA382536400
NM_000051.4:c.1915G>C