Canonical Allele Identifier: PA2826462727
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 820647
ClinVar RCV Id: RCV001014309 RCV001059229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro3Arg
CA46667221
NM_001258281.1:c.8C>G