Canonical Allele Identifier: PA2825030360
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1001382
ClinVar RCV Id: RCV001297669
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Arg189Ser
CA382527825
NM_000051.4:c.567A>C
CA382527826
NM_000051.4:c.567A>T