Canonical Allele Identifier: PA2826465511
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182579
ClinVar RCV Id: RCV000160611 RCV000212618 RCV000542071 RCV000656881 RCV001357332
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln727Glu
CA020523
NM_001258281.1:c.2179C>G