Canonical Allele Identifier: PA165925
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser328Arg
CA016753
NM_000179.3:c.984C>G
CA346741028
NM_000179.3:c.982A>C
CA346741061
NM_000179.3:c.984C>A