Canonical Allele Identifier: PA2826627649
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477364
ClinVar RCV Id: RCV001971558 RCV002256878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val760Asp
CA346755239
NM_001281492.2:c.2279T>A