Canonical Allele Identifier: PA658672596
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483664
ClinVar RCV Id: RCV000570315 RCV000802215 RCV001310202 RCV002497211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser554Asn
CA030195
NM_000251.3:c.1661G>A