Canonical Allele Identifier: PA2826625758
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89188
ClinVar RCV Id: RCV000074650
ClinVar Variation Id: 2859099
ClinVar RCV Id: RCV003759249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu316Asp
CA008501
NM_001281492.2:c.948A>T
CA346744577
NM_001281492.2:c.948A>C