Canonical Allele Identifier: PA658736932
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_000042.3:p.Ser328Arg
CA382531145
NM_000051.4:c.982A>C
CA382531197
NM_000051.4:c.984T>A
CA382531198
NM_000051.4:c.984T>G