Canonical Allele Identifier: PA915984221
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91097
ClinVar RCV Id: RCV000148628 RCV000115532 RCV000212585 RCV000764421 RCV000662480 RCV000588226 RCV001262752 RCV001085983 RCV001798267 RCV001358588 RCV004528278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile79Met
CA021158
NM_001258281.1:c.237T>G