Canonical Allele Identifier: PA913192098
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628958
ClinVar RCV Id: RCV000773625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys479Thr
CA346745564
NM_000179.3:c.1436A>C