Canonical Allele Identifier: PA2826463435
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 126976
ClinVar RCV Id: RCV000114837 RCV000115546 RCV000699802 RCV001800400 RCV003997208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr226Ser
CA022468
NM_001258281.1:c.676A>T
CA346732887
NM_001258281.1:c.677C>G