Canonical Allele Identifier: PA2826462837
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489943
ClinVar RCV Id: RCV000580951 RCV000629862 RCV001090210 RCV001193290 RCV004001260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg30Cys
CA346729600
NM_001258281.1:c.88C>T