Canonical Allele Identifier: PA2826630296
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 932698
ClinVar RCV Id: RCV001200626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu191Lys
CA346745983
NM_001281493.2:c.571G>A