Canonical Allele Identifier: PA2825088957
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2741883
ClinVar RCV Id: RCV003593519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu639Gln
CA346750219
NM_000179.3:c.1915G>C