Canonical Allele Identifier: PA2826637343
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994636
ClinVar RCV Id: RCV002791280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg774_Pro775insSer
CA2580066980
NM_001281494.2:c.2322_2323insAGC