Canonical Allele Identifier: PA645472103
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408483
ClinVar RCV Id: RCV000473312 RCV000587461 RCV001026892
ClinVar Variation Id: 921168
ClinVar RCV Id: RCV001180427 RCV001316892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu262Asp
CA040426
NM_000251.3:c.786G>C
CA16611010
NM_000251.3:c.786G>T