Canonical Allele Identifier: PA165359
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89396
ClinVar RCV Id: RCV000129922 RCV001370905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1160Leu
CA013040
NM_000179.3:c.3478G>C