Canonical Allele Identifier: PA2826463321
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91208
ClinVar RCV Id: RCV000076712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln198His
CA022289
NM_001258281.1:c.594G>C
CA346732533
NM_001258281.1:c.594G>T