Canonical Allele Identifier: PA2826627378
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014625
ClinVar RCV Id: RCV001313382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His696Gln
CA346754156
NM_001281492.2:c.2088T>A
CA346754158
NM_001281492.2:c.2088T>G