Canonical Allele Identifier: PA2826464287
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185360
ClinVar RCV Id: RCV000164768 RCV000167935 RCV000486548 RCV003995363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr429Ile
CA018409
NM_001258281.1:c.1286C>T