Canonical Allele Identifier: PA2826626854
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89252
ClinVar RCV Id: RCV001360931 RCV002415522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu570Phe
CA009680
NM_001281492.2:c.1708C>T