Canonical Allele Identifier: PA2826636009
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845264
ClinVar RCV Id: RCV001048297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr465_Pro466del
CA916079957
NM_001281494.2:c.1393_1398del