Canonical Allele Identifier: PA2826632382
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630731
ClinVar RCV Id: RCV000776701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu677Val
CA346756210
NM_001281493.2:c.2029C>G