Canonical Allele Identifier: PA916011014
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232287
ClinVar RCV Id: RCV000222952 RCV000471165 RCV003997958
ClinVar Variation Id: 548780
ClinVar RCV Id: RCV000662729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Trp50Cys
CA10578025
NM_001281492.2:c.150G>C
CA346734938
NM_001281492.2:c.150G>T