Canonical Allele Identifier: PA2826464762
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184308
ClinVar RCV Id: RCV000163537 RCV000484226 RCV000657098 RCV000794229 RCV003467279 RCV003995260
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His544Tyr
CA019408
NM_001258281.1:c.1630C>T