Canonical Allele Identifier: PA2826628878
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231211
ClinVar RCV Id: RCV000220341 RCV000552496 RCV001775683 RCV003224227 RCV003997889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1118Tyr
CA071942
NM_001281492.2:c.3352C>T