Canonical Allele Identifier: PA357764
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220619
ClinVar RCV Id: RCV000206842 RCV000220316 RCV000482863 RCV001034622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met1144Arg
CA350840
NM_000179.3:c.3431T>G