Canonical Allele Identifier: PA2499245063
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058623
ClinVar RCV Id: RCV001367783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro38His
CA346734856
NM_001281492.2:c.113C>A