Canonical Allele Identifier: PA645475571
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408544
ClinVar RCV Id: RCV000573097 RCV000464961 RCV000781562 RCV001788225 RCV004000793 RCV003228932
ClinVar Variation Id: 491802
ClinVar RCV Id: RCV000583000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr756Ser
CA035142
NM_000251.3:c.2267C>G
CA46704862
NM_000251.3:c.2266A>T