Canonical Allele Identifier: PA916011016
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187071
ClinVar RCV Id: RCV000166759 RCV000203855 RCV001358151 RCV001548024 RCV002281987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Trp50Arg
CA008708
NM_001281492.2:c.148T>C
CA346734933
NM_001281492.2:c.148T>A