Canonical Allele Identifier: PA2826635958
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1013697
ClinVar RCV Id: RCV001312322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu453Lys
CA346752768
NM_001281494.2:c.1357G>A