Canonical Allele Identifier: PA299435
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182623
ClinVar RCV Id: RCV000160668 RCV000560061 RCV000571101 RCV000708869 RCV000767214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg554His
CA009015
NM_000179.3:c.1661G>A