Canonical Allele Identifier: PA2826635749
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89254
ClinVar RCV Id: RCV000074718 RCV001530136 RCV003137606 RCV001854277 RCV003584540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe404Ser
CA009702
NM_001281494.2:c.1211T>C