Canonical Allele Identifier: PA2826465753
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479836
ClinVar RCV Id: RCV000574140 RCV000679307 RCV000694840 RCV003470822 RCV004000859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile791Val
CA036657
NM_001258281.1:c.2371A>G