Canonical Allele Identifier: PA913192384
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630831
ClinVar RCV Id: RCV000776835 RCV000815193
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser238Cys
CA346739996
NM_000179.3:c.713C>G