Canonical Allele Identifier: PA916032847
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 141488
ClinVar RCV Id: RCV000130042 RCV000442870 RCV000700863
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu1277Asp
CA165593
NM_001351834.2:c.3831G>C
CA382524964
NM_001351834.2:c.3831G>T