Canonical Allele Identifier: PA2826632831
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009182
ClinVar RCV Id: RCV001306638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro780Thr
CA346758109
NM_001281493.2:c.2338C>A