Canonical Allele Identifier: PA339028
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216348
ClinVar RCV Id: RCV000199994 RCV000410314 RCV000485278 RCV000490871 RCV000767061 RCV003997017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly683Val
CA339026
NM_000251.3:c.2048G>T