Canonical Allele Identifier: PA2826627046
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 948777
ClinVar RCV Id: RCV001220101 RCV002418756 RCV003462747
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn618Ser
CA346752616
NM_001281492.2:c.1853A>G