Canonical Allele Identifier: PA2825033987
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1430992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Glu1800Asp
CA382543733
NM_000051.4:c.5400A>C
CA382543735
NM_000051.4:c.5400A>T