Canonical Allele Identifier: PA891846356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 580297
ClinVar RCV Id: RCV000703787 RCV001021464 RCV003128652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu1311dup
CA1649481
NM_000179.3:c.3932_3934dup