Canonical Allele Identifier: PA2826637355
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 920941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu779Phe
CA346758104
NM_001281494.2:c.2337G>C
CA346758106
NM_001281494.2:c.2337G>T