Canonical Allele Identifier: PA2826465277
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820841
ClinVar RCV Id: RCV001014690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu665Asp
CA346729408
NM_001258281.1:c.1995A>C
CA346729409
NM_001258281.1:c.1995A>T