Canonical Allele Identifier: PA2826465797
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408526
ClinVar RCV Id: RCV000580161 RCV000460192 RCV003317217 RCV004000789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile799Thr
CA036766
NM_001258281.1:c.2396T>C