Canonical Allele Identifier: PA2826630658
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134852
ClinVar RCV Id: RCV000121579 RCV000131162 RCV000204422 RCV000410866 RCV000587914 RCV000708870 RCV001249972 RCV001355523 RCV001762265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg275His
CA009094
NM_001281493.2:c.824G>A