Canonical Allele Identifier: PA2826629188
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736197
ClinVar RCV Id: RCV002373181
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn1177Ile
CA346761459
NM_001281492.2:c.3530A>T