Canonical Allele Identifier: PA1139673282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 932698
ClinVar RCV Id: RCV001200626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu493Lys
CA346745983
NM_000179.3:c.1477G>A