Canonical Allele Identifier: PA2826624870
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142508
ClinVar RCV Id: RCV000131657 RCV000214572 RCV000410793 RCV000472070 RCV000656889 RCV003467180 RCV003998114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser108Tyr
CA016318
NM_001281492.2:c.323C>A