Canonical Allele Identifier: PA2826635489
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1098783
ClinVar RCV Id: RCV001420816 RCV001865910 RCV003365385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys344Glu
CA346750422
NM_001281494.2:c.1030A>G