Canonical Allele Identifier: PA916011439
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127585
ClinVar RCV Id: RCV000115413 RCV000121585 RCV000204658 RCV000412360 RCV000586502 RCV001080360 RCV001798330 RCV003460816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg965Cys
CA012434
NM_001281492.2:c.2893C>T