Canonical Allele Identifier: PA2825091888
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587333
ClinVar RCV Id: RCV003360811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1198Ser
CA346760538
NM_000179.3:c.3592G>T