Canonical Allele Identifier: PA2826625387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485878
ClinVar RCV Id: RCV000566365 RCV002469207 RCV001229506 RCV004001123
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp228Glu
CA067120
NM_001281492.2:c.684C>G
CA346741706
NM_001281492.2:c.684C>A