Canonical Allele Identifier: PA2826635850
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89260
ClinVar RCV Id: RCV000221222 RCV000563245 RCV000688768 RCV000657127 RCV003997073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys426Thr
CA009828
NM_001281494.2:c.1277A>C