Canonical Allele Identifier: PA2826628486
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525734
ClinVar RCV Id: RCV000629978
ClinVar Variation Id: 823848
ClinVar RCV Id: RCV001020447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1036Ser
CA346760164
NM_001281492.2:c.3108G>C
CA346760165
NM_001281492.2:c.3108G>T