Canonical Allele Identifier: PA2826628591
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 490005
ClinVar RCV Id: RCV000580926
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1057Gln
CA346760411
NM_001281492.2:c.3169G>C