Canonical Allele Identifier: PA2826634314
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser26Arg
CA016753
NM_001281494.2:c.78C>G
CA346741028
NM_001281494.2:c.76A>C
CA346741061
NM_001281494.2:c.78C>A