Canonical Allele Identifier: PA2826625694
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428381
ClinVar RCV Id: RCV000491842 RCV001851340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly300Glu
CA346744168
NM_001281492.2:c.899G>A