Canonical Allele Identifier: PA915963068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 822931
ClinVar RCV Id: RCV001018708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro104His
CA346736824
NM_000179.3:c.311C>A