Canonical Allele Identifier: PA2826637160
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186021
ClinVar RCV Id: RCV000165541 RCV000410356 RCV000483409 RCV000685194 RCV002267913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr736Cys
CA011594
NM_001281494.2:c.2207A>G