Canonical Allele Identifier: PA2826633091
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 650516
ClinVar Variation Id: 2453170
ClinVar RCV Id: RCV003182625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly836Arg
CA346758906
NM_001281493.2:c.2506G>A
CA346758908
NM_001281493.2:c.2506G>C