Canonical Allele Identifier: PA2826635297
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165988
ClinVar RCV Id: RCV003090265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys301Glu
CA346749367
NM_001281494.2:c.901A>G