Canonical Allele Identifier: PA2825087510
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2108380
ClinVar RCV Id: RCV003034149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys324Ile
CA346740953
NM_000179.3:c.971A>T