Canonical Allele Identifier: PA658672766
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455528
ClinVar RCV Id: RCV000549787 RCV000663143 RCV000575117 RCV000758651 RCV001764525
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg621Gln
CA031795
NM_000251.3:c.1862G>A