Canonical Allele Identifier: PA331428
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90854
ClinVar RCV Id: RCV000076356 RCV000491447 RCV000581599 RCV000692084 RCV002477219 RCV003452879
ClinVar Variation Id: 1784315
ClinVar RCV Id: RCV002417252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly669Val
CA019785
NM_000251.3:c.2006G>T
CA2580067124
NM_000251.3:c.2006_2007delinsTT