Canonical Allele Identifier: PA189706
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184688
ClinVar RCV Id: RCV000163983 RCV000473165 RCV003462124 RCV003995306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln344His
CA016922
NM_000251.3:c.1032G>C
CA346733189
NM_000251.3:c.1032G>T