Canonical Allele Identifier: PA916011068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410493
ClinVar RCV Id: RCV000470612 RCV000776536 RCV000485693 RCV004001846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro66Leu
CA16611077
NM_001281492.2:c.197C>T