Canonical Allele Identifier: PA211684
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89571
ClinVar RCV Id: RCV000148648 RCV000160657 RCV000212635 RCV000556949 RCV001174593 RCV003997105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser285Ile
CA016543
NM_000179.3:c.854G>T