Canonical Allele Identifier: PA357316
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220279
ClinVar RCV Id: RCV000204000 RCV000491184 RCV000662780 RCV000587576 RCV003997628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp89Glu
CA069427
NM_000179.3:c.267C>G
CA346736470
NM_000179.3:c.267C>A