Canonical Allele Identifier: PA916011164
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127604
ClinVar RCV Id: RCV000115441 RCV000410116 RCV000466432 RCV000566072 RCV003467044 RCV003997255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu98Lys
CA016246
NM_001281492.2:c.292G>A