Canonical Allele Identifier: PA354484
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_000170.1:p.Asp1058His
CA279731
NM_000179.3:c.3172G>C