Canonical Allele Identifier: PA163775
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140864
ClinVar RCV Id: RCV000129078 RCV000210120 RCV000482497 RCV000524342 RCV000662718 RCV000781551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys449Asn
CA018049
NM_000251.3:c.1347G>C
CA346724703
NM_000251.3:c.1347G>T