Canonical Allele Identifier: PA916031560
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 490759
ClinVar RCV Id: RCV000581170 RCV001860070
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser328Arg
CA382531145
NM_001351834.2:c.982A>C
CA382531197
NM_001351834.2:c.984T>A
CA382531198
NM_001351834.2:c.984T>G