Canonical Allele Identifier: PA1139691055
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 933158
ClinVar RCV Id: RCV001201191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr945Ile
CA346761055
NM_001281494.2:c.2834C>T