Canonical Allele Identifier: PA2826634836
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 819349
ClinVar RCV Id: RCV001011829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Cys194Ser
CA346746068
NM_001281494.2:c.580T>A
CA346746071
NM_001281494.2:c.581G>C