Canonical Allele Identifier: PA2825089392
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2803672
ClinVar RCV Id: RCV003760709

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn751His
CA346752660
NM_000179.3:c.2251A>C