Canonical Allele Identifier: PA2573163093
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352094
ClinVar RCV Id: RCV002047340 RCV002388706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp253His
CA346740143
NM_000179.3:c.757G>C