Canonical Allele Identifier: PA2826627100
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423154
ClinVar RCV Id: RCV001926520
ClinVar Variation Id: 2767129
ClinVar RCV Id: RCV003594493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu630Asp
CA346752883
NM_001281492.2:c.1890G>C
CA346752885
NM_001281492.2:c.1890G>T