Canonical Allele Identifier: PA2826632609
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428405
ClinVar RCV Id: RCV000490990 RCV000659893 RCV001865529 RCV000521749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met731Lys
CA346756599
NM_001281493.2:c.2192T>A