Canonical Allele Identifier: PA2825092634
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2738992
ClinVar RCV Id: RCV003593443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1302Val
CA346761434
NM_000179.3:c.3905C>T