Canonical Allele Identifier: PA645379387
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser346Cys
CA16610875
NM_000179.3:c.1037C>G