Canonical Allele Identifier: PA2825087431
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1983475
ClinVar RCV Id: RCV002770293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg316Ser
CA346740809
NM_000179.3:c.948G>C
CA346740811
NM_000179.3:c.948G>T