Canonical Allele Identifier: PA2826465173
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233375
ClinVar RCV Id: RCV000222410 RCV000227730 RCV000411876 RCV000708841 RCV000483732 RCV001356541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile638Thr
CA033790
NM_001258281.1:c.1913T>C