Canonical Allele Identifier: PA2826626260
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89217
ClinVar RCV Id: RCV000131251 RCV000212651 RCV000411714 RCV001080487 RCV001328467 RCV004542740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly436Arg
CA009071
NM_001281492.2:c.1306G>A
CA346747544
NM_001281492.2:c.1306G>C