Canonical Allele Identifier: PA2826462733
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 852426
ClinVar RCV Id: RCV001057027
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala4Ser
CA346729063
NM_001258281.1:c.10G>T