Canonical Allele Identifier: PA2825092093
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 843701
ClinVar RCV Id: RCV001046379 RCV003283890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1232Ile
CA346760966
NM_000179.3:c.3694G>A