Canonical Allele Identifier: PA2825091980
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 956952
ClinVar RCV Id: RCV001229851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1213His
CA346760614
NM_000179.3:c.3637G>C