Canonical Allele Identifier: PA166758
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141908
ClinVar RCV Id: RCV000130615 RCV001219936 RCV001356288 RCV003998069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr336Ser
CA007788
NM_000179.3:c.1007C>G
CA346741238
NM_000179.3:c.1006A>T