Canonical Allele Identifier: PA2826463731
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90539
ClinVar RCV Id: RCV000076034 RCV001230748 RCV002415553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg293Ser
CA017208
NM_001258281.1:c.879A>T
CA346733519
NM_001258281.1:c.879A>C