Canonical Allele Identifier: PA160903
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134852
ClinVar RCV Id: RCV000121579 RCV000131162 RCV000204422 RCV000410866 RCV000587914 RCV000708870 RCV001249972 RCV001355523 RCV001762265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg577His
CA009094
NM_000179.3:c.1730G>A