Canonical Allele Identifier: PA2826635483
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89233
ClinVar RCV Id: RCV000074697 RCV000166227 RCV000219792 RCV000409155 RCV000524127 RCV001355116 RCV001703971 RCV004537274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg342Ser
CA009475
NM_001281494.2:c.1026G>C
CA346750390
NM_001281494.2:c.1026G>T