Canonical Allele Identifier: PA330540
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1201Val
CA013502
NM_000179.3:c.3601C>G