Canonical Allele Identifier: PA658802581
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525848
ClinVar RCV Id: RCV000630193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1313_Gln1314insHisIle
CA658795758
NM_000179.3:c.3936_3941dup