Canonical Allele Identifier: PA2826635521
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514670
ClinVar RCV Id: RCV002029468
ClinVar Variation Id: 1783420
ClinVar RCV Id: RCV002421729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met352Leu
CA346750579
NM_001281494.2:c.1054A>T
CA346750581
NM_001281494.2:c.1054A>C