Canonical Allele Identifier: PA2499229338
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1054176
ClinVar RCV Id: RCV001362636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu778His
CA346753381
NM_000179.3:c.2333T>A