Canonical Allele Identifier: PA2826627038
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 575310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile615Val
CA068641
NM_001281492.2:c.1843A>G