Canonical Allele Identifier: PA916011732
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127554
ClinVar RCV Id: RCV000115368 RCV000210148 RCV000212645 RCV000415687 RCV000528613 RCV000662663 RCV001193101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr67Ile
CA008045
NM_001281494.2:c.200C>T