Canonical Allele Identifier: PA2826626663
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474116
ClinVar RCV Id: RCV001971032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val528Leu
CA346750606
NM_001281492.2:c.1582G>T
CA346750607
NM_001281492.2:c.1582G>C