Canonical Allele Identifier: PA2825092622
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736032
ClinVar RCV Id: RCV002373095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn1301Ile
CA346761426
NM_000179.3:c.3902A>T