Canonical Allele Identifier: PA2826626317
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 572941
ClinVar RCV Id: RCV000694465 RCV003999615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His448Arg
CA346748791
NM_001281492.2:c.1343A>G