Canonical Allele Identifier: PA916011109
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455187
ClinVar RCV Id: RCV000525000 RCV000561728 RCV000759131 RCV003153676 RCV004003675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg77Trp
CA068784
NM_001281492.2:c.229C>T