Canonical Allele Identifier: PA2826625201
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 951825
ClinVar RCV Id: RCV001223820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser185Phe
CA46707062
NM_001281492.2:c.554C>T