Canonical Allele Identifier: PA287470
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127654
ClinVar RCV Id: RCV000115544 RCV000472973 RCV000212593 RCV001193849 RCV000663090
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp282Gly
CA022423
NM_000251.3:c.845A>G