Canonical Allele Identifier: PA2826587546
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525655
ClinVar RCV Id: RCV000629807 RCV001526019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser1038_Thr1042del
CA658795767
NM_001281494.2:c.3112_3126del