Canonical Allele Identifier: PA2826632885
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479930
ClinVar RCV Id: RCV000575395 RCV001770503 RCV001858111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu788Gln
CA346758204
NM_001281493.2:c.2362G>C