Canonical Allele Identifier: PA2826635711
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2116355
ClinVar RCV Id: RCV003034964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu393Arg
CA346750836
NM_001281494.2:c.1178T>G