Canonical Allele Identifier: PA211690
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89281
ClinVar RCV Id: RCV000148651 RCV000130124 RCV000212666 RCV000410826 RCV000586083 RCV000524143 RCV001356592 RCV003466944 RCV003997077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp803Gly
CA010206
NM_000179.3:c.2408A>G