Canonical Allele Identifier: PA2826465090
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90873
ClinVar RCV Id: RCV000160600 RCV000524374 RCV000586744 RCV003452885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu621Pro
CA019927
NM_001258281.1:c.1862T>C