Canonical Allele Identifier: PA2826465527
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216355
ClinVar RCV Id: RCV000200437 RCV000216489 RCV001577165 RCV003997021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr730Ile
CA339316
NM_001258281.1:c.2189C>T