Canonical Allele Identifier: PA658802198
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525817
ClinVar RCV Id: RCV000630145 RCV003465388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp697His
CA346750852
NM_000179.3:c.2089G>C