Canonical Allele Identifier: PA2826629107
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046250
ClinVar RCV Id: RCV001350787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly1162Arg
CA346761364
NM_001281492.2:c.3484G>C
CA346761365
NM_001281492.2:c.3484G>A