Canonical Allele Identifier: PA2826464996
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037505
ClinVar RCV Id: RCV001340669 RCV003469568
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile600Val
CA346728936
NM_001258281.1:c.1798A>G