Canonical Allele Identifier: PA2826465432
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90955
ClinVar RCV Id: RCV000076457 RCV000217041 RCV000410216 RCV000524385 RCV000586175 RCV001804168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile704Val
CA020467
NM_001258281.1:c.2110A>G