Canonical Allele Identifier: PA915983998
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91061
ClinVar RCV Id: RCV000478164 RCV000491016 RCV000662774 RCV001232251 RCV003997171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr37Cys
CA021001
NM_001258281.1:c.110A>G