Canonical Allele Identifier: PA192567
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185667
ClinVar RCV Id: RCV000165125 RCV000459296 RCV001527033 RCV003995394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1261Val
CA014254
NM_000179.3:c.3782C>T