Canonical Allele Identifier: PA2826465968
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216359
ClinVar RCV Id: RCV000198941 RCV000223226 RCV000235290 RCV000412048 RCV003997023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys843Ile
CA037340
NM_001258281.1:c.2528A>T