Canonical Allele Identifier: PA193389
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185923
ClinVar RCV Id: RCV000165428 RCV001308320 RCV002284369 RCV003462171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile258Val
CA016458
NM_000179.3:c.772A>G