Canonical Allele Identifier: PA2826465326
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439191
ClinVar RCV Id: RCV000507559 RCV001219215 RCV001250042 RCV002431464 RCV003449448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser677Leu
CA346729718
NM_001258281.1:c.2030C>T