Canonical Allele Identifier: PA916011130
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220192
ClinVar RCV Id: RCV000204219 RCV000216919 RCV000588780 RCV003997621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr86Ile
CA073299
NM_001281492.2:c.257C>T