Canonical Allele Identifier: PA2826624850
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 937367
ClinVar RCV Id: RCV001206362 RCV002365931 RCV004010645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro103Leu
CA346739964
NM_001281492.2:c.308C>T