Canonical Allele Identifier: PA2826626756
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230009
ClinVar RCV Id: RCV000213514 RCV000529803 RCV000985829 RCV003468992 RCV003997791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu548Gln
CA068389
NM_001281492.2:c.1642G>C