Canonical Allele Identifier: PA2825091937
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823993
ClinVar RCV Id: RCV001020730 RCV001860995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1205Lys
CA346760576
NM_000179.3:c.3614C>A