Canonical Allele Identifier: PA2826634840
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 650552
ClinVar Variation Id: 1773857
ClinVar RCV Id: RCV002389774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys196Asn
CA346746138
NM_001281494.2:c.588G>C
CA346746139
NM_001281494.2:c.588G>T