Canonical Allele Identifier: PA2825086370
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701657
ClinVar RCV Id: RCV003594920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala182Ser
CA346738733
NM_000179.3:c.544G>T