Canonical Allele Identifier: PA165037
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141296
ClinVar RCV Id: RCV000129763 RCV000204094 RCV000410024 RCV002288628 RCV003997522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr969Phe
CA011081
NM_000179.3:c.2906A>T