Canonical Allele Identifier: PA645383708
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 421879
ClinVar RCV Id: RCV000482150 RCV000570886 RCV000560746 RCV004003362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro1086His
CA070513
NM_000179.3:c.3257C>A