Canonical Allele Identifier: PA2826635043
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 917822
ClinVar RCV Id: RCV001175088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu242Val
CA346747155
NM_001281494.2:c.725A>T