Canonical Allele Identifier: PA2826633466
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043781
ClinVar RCV Id: RCV001751677 RCV001347940 RCV002456509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala918Thr
CA071802
NM_001281493.2:c.2752G>A