Canonical Allele Identifier: PA645503191
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 424994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys1811Ser
CA16621628
NM_000051.4:c.5432G>C
CA382544010
NM_000051.4:c.5431T>A