Canonical Allele Identifier: PA2826628851
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89449
ClinVar RCV Id: RCV000216969 RCV000684809 RCV000767045 RCV004017385 RCV003460689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1112Ser
CA014030
NM_001281492.2:c.3334C>A