Canonical Allele Identifier: PA2825089375
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050489
ClinVar RCV Id: RCV002921931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu747Val
CA346752579
NM_000179.3:c.2239C>G