Canonical Allele Identifier: PA2826465725
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90998
ClinVar RCV Id: RCV000236323 RCV000410329 RCV000491427 RCV000552050 RCV002247471 RCV003153357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu785Ile
CA020709
NM_001258281.1:c.2353C>A