Canonical Allele Identifier: PA2825091957
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372729
ClinVar RCV Id: RCV001874785 RCV002458693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser1208Tyr
CA346760593
NM_000179.3:c.3623C>A