Canonical Allele Identifier: PA2826633746
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141916
ClinVar RCV Id: RCV000130625 RCV000589175 RCV001086478 RCV001260255 RCV003998071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro976Thr
CA014466
NM_001281493.2:c.2926C>A