Canonical Allele Identifier: PA2826632449
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 439206
ClinVar RCV Id: RCV000507674 RCV001183217 RCV000699493 RCV003464091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu691Asp
CA346756354
NM_001281493.2:c.2073A>C
CA346756355
NM_001281493.2:c.2073A>T