Canonical Allele Identifier: PA2826626007
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774467
ClinVar RCV Id: RCV002392469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val378Leu
CA346746400
NM_001281492.2:c.1132G>C
CA346746401
NM_001281492.2:c.1132G>T