Canonical Allele Identifier: PA2825089567
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790367
ClinVar RCV Id: RCV002457830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp793Phe
CA2580067841
NM_000179.3:c.2377_2378delinsTT