Canonical Allele Identifier: PA294211
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141874
ClinVar RCV Id: RCV000130571 RCV000235178 RCV000475467 RCV001527050 RCV003998064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser9Gly
CA010478
NM_000179.3:c.25A>G