Canonical Allele Identifier: PA2826636019
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89266
ClinVar RCV Id: RCV000491736 RCV001203081 RCV001545670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro466del
CA009988
NM_001281494.2:c.1396_1398del