Canonical Allele Identifier: PA2499230042
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051098
ClinVar RCV Id: RCV001359090 RCV003298563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg638Ser
CA346728644
NM_000251.3:c.1914G>C
CA346728647
NM_000251.3:c.1914G>T