Canonical Allele Identifier: PA2826629505
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 663267
ClinVar RCV Id: RCV000821117
ClinVar Variation Id: 1318688
ClinVar RCV Id: RCV001768312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr3Ser
CA346740725
NM_001281493.2:c.7A>T
CA346740727
NM_001281493.2:c.8C>G