Canonical Allele Identifier: PA2826637315
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly770Val
CA011990
NM_001281494.2:c.2309G>T