Canonical Allele Identifier: PA2826627194
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 433914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro651Leu
CA346753452
NM_001281492.2:c.1952C>T