Canonical Allele Identifier: PA2825092069
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462508
ClinVar RCV Id: RCV001954276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1228Val
CA346760916
NM_000179.3:c.3683C>T