Canonical Allele Identifier: PA2827630147
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 660737
ClinVar RCV Id: RCV000817994 RCV001176201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Arg76Ser
CA382521446
NM_001351835.2:c.228A>T
CA382521449
NM_001351835.2:c.228A>C