Canonical Allele Identifier: PA2573163265
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1684900
ClinVar RCV Id: RCV002247992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile464Val
CA346745102
NM_000179.3:c.1390A>G