Canonical Allele Identifier: PA2826633626
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val951Ile
CA10578159
NM_001281493.2:c.2851G>A