Canonical Allele Identifier: PA916010902
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821688
ClinVar RCV Id: RCV001016350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser9Thr
CA346734507
NM_001281492.2:c.26G>C