Canonical Allele Identifier: PA299497
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 36596
ClinVar RCV Id: RCV000030274 RCV000160705 RCV000569787 RCV000662751 RCV000627725 RCV001818192 RCV003466879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys13Thr
CA014649
NM_000179.3:c.38A>C