Canonical Allele Identifier: PA190063
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184794
ClinVar RCV Id: RCV000164110 RCV000506000 RCV000466573 RCV000589252 RCV000663282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1160Phe
CA013053
NM_000179.3:c.3478G>T