Canonical Allele Identifier: PA2826625101
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 959901
ClinVar RCV Id: RCV001233333 RCV002375242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser162Gly
CA346740648
NM_001281492.2:c.484A>G