Canonical Allele Identifier: PA891846185
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 581776
ClinVar RCV Id: RCV000705699 RCV002442532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser806Phe
CA346754006
NM_000179.3:c.2417C>T