Canonical Allele Identifier: PA2826624883
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380166
ClinVar RCV Id: RCV001917150 RCV003164268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser112Asn
CA346740017
NM_001281492.2:c.335G>A