Canonical Allele Identifier: PA2826634764
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467382
ClinVar RCV Id: RCV001990759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys177Gln
CA346745543
NM_001281494.2:c.529A>C