Canonical Allele Identifier: PA193626
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186012
ClinVar RCV Id: RCV000165532 RCV002516483 RCV003995423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val890Leu
CA010714
NM_000179.3:c.2668G>C