Canonical Allele Identifier: PA658680801
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu671Phe
CA346750687
NM_000179.3:c.2013G>T
CA346750688
NM_000179.3:c.2013G>C