Canonical Allele Identifier: PA916012170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu935Asp
CA013945
NM_001281494.2:c.2805G>C
CA346761001
NM_001281494.2:c.2805G>T