Canonical Allele Identifier: PA2826636138
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_001268423.1:p.Asp495Glu
CA346753843
NM_001281494.2:c.1485C>A
CA346753846
NM_001281494.2:c.1485C>G