Canonical Allele Identifier: PA658680774
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu638Val
CA346750196
NM_000179.3:c.1912C>G
CA658655795
NM_000179.3:c.1911_1912delinsTG