Canonical Allele Identifier: PA916011540
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 584615
ClinVar RCV Id: RCV000708860 RCV001861934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly6Ala
CA346740745
NM_001281494.2:c.17G>C