Canonical Allele Identifier: PA165904
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89251
ClinVar RCV Id: RCV000130187 RCV000480300 RCV000524131 RCV000662368 RCV003320553 RCV003466939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln698Glu
CA009674
NM_000179.3:c.2092C>G