Canonical Allele Identifier: PA167647
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91063
ClinVar RCV Id: RCV000131126 RCV000811372 RCV003317079 RCV003466967 RCV003997172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala107Pro
CA021012
NM_000251.3:c.319G>C