Canonical Allele Identifier: PA167929
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142270
ClinVar RCV Id: RCV000131293 RCV000234661 RCV001560125 RCV003398768 RCV003998098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr1066Cys
CA011852
NM_000179.3:c.3197A>G