Canonical Allele Identifier: PA2825089139
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2421160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala680Pro
CA346750738
NM_000179.3:c.2038G>C