Canonical Allele Identifier: PA2826465291
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455550
ClinVar RCV Id: RCV000532179 RCV000568631 RCV001755787 RCV004003742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser668Cys
CA346729424
NM_001258281.1:c.2003C>G