Canonical Allele Identifier: PA2826631070
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784361
ClinVar RCV Id: RCV002417298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly368Arg
CA009551
NM_001281493.2:c.1102G>A
CA346750677
NM_001281493.2:c.1102G>C