Canonical Allele Identifier: PA2826625118
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321106
ClinVar RCV Id: RCV001777085 RCV001868819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val166Phe
CA346740678
NM_001281492.2:c.496G>T