ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826628737
Gene: MSH6
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1060721
ClinVar RCV Id:
RCV001370187
RCV002456578
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268421.1:p.Ala1090Val
CA346760831
NM_001281492.2:c.3269C>T