Canonical Allele Identifier: PA916011332
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 218057
ClinVar RCV Id: RCV000202089 RCV000501351 RCV000491378 RCV001039124 RCV001353871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp928His
CA279731
NM_001281492.2:c.2782G>C