Canonical Allele Identifier: PA2825090901
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994636
ClinVar RCV Id: RCV002791280

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1076_Pro1077insSer
CA2580066980
NM_000179.3:c.3228_3229insAGC