Canonical Allele Identifier: PA2826463187
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455608
ClinVar RCV Id: RCV000559155 RCV001025957 RCV002248760 RCV001770405 RCV004003754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys169Glu
CA040162
NM_001258281.1:c.505A>G