Canonical Allele Identifier: PA891844987
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 575868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His635Gln
CA382536291
NM_000051.4:c.1905C>A
CA382536294
NM_000051.4:c.1905C>G