Canonical Allele Identifier: PA915983949
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 666142
ClinVar RCV Id: RCV000824574
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val34Ile
CA346729621
NM_001258281.1:c.100G>A