Canonical Allele Identifier: PA2825089158
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2045194
ClinVar RCV Id: RCV002918001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys687Tyr
CA346750776
NM_000179.3:c.2060G>A