Canonical Allele Identifier: PA330625
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile251Met
CA016429
NM_000179.3:c.753A>G