Canonical Allele Identifier: PA915965066
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821198
ClinVar RCV Id: RCV001015377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp797Glu
CA346753843
NM_000179.3:c.2391C>A
CA346753846
NM_000179.3:c.2391C>G