Canonical Allele Identifier: PA916012089
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234147
ClinVar RCV Id: RCV000218868 RCV000553146 RCV000985846 RCV004532808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His901Tyr
CA10578151
NM_001281494.2:c.2701C>T