Canonical Allele Identifier: PA916011985
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823881
ClinVar RCV Id: RCV001020518
ClinVar Variation Id: 1347029
ClinVar RCV Id: RCV002032950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe872Leu
CA346760210
NM_001281494.2:c.2614T>C
CA346760215
NM_001281494.2:c.2616T>A
CA346760216
NM_001281494.2:c.2616T>G