Canonical Allele Identifier: PA2826626879
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 920662
ClinVar RCV Id: RCV001179518
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu577Asp
CA346750990
NM_001281492.2:c.1731A>C
CA346750992
NM_001281492.2:c.1731A>T