Canonical Allele Identifier: PA916011878
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 665466
ClinVar RCV Id: RCV000823760 RCV001020244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly837Cys
CA346758916
NM_001281494.2:c.2509G>T