Canonical Allele Identifier: PA2826635087
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410498
ClinVar RCV Id: RCV000473757 RCV000580839 RCV001030493 RCV001566013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg252Cys
CA067976
NM_001281494.2:c.754C>T