Canonical Allele Identifier: PA167742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89219
ClinVar RCV Id: RCV000131189 RCV000485534 RCV000524119 RCV001818236 RCV002498356 RCV003466936 RCV004019093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser580Leu
CA009108
NM_000179.3:c.1739C>T