Canonical Allele Identifier: PA2825089091
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784279
ClinVar RCV Id: RCV002417216 RCV004007388
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser668Cys
CA346750671
NM_000179.3:c.2003C>G