Canonical Allele Identifier: PA2826633264
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 938809
ClinVar RCV Id: RCV001208100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu875Arg
CA346760230
NM_001281493.2:c.2624T>G