Canonical Allele Identifier: PA658680809
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485871
ClinVar RCV Id: RCV000564526 RCV001070185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu681Phe
CA346750745
NM_000179.3:c.2041C>T