Canonical Allele Identifier: PA2826628959
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025468
ClinVar RCV Id: RCV001325782 RCV002366203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1136Asp
CA346761188
NM_001281492.2:c.3406C>G