Canonical Allele Identifier: PA2499245105
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171277
ClinVar RCV Id: RCV001524238 RCV001872024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro41His
CA346741378
NM_001281494.2:c.122C>A