Canonical Allele Identifier: PA915965218
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821928
ClinVar RCV Id: RCV001016842 RCV002550823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr966Ser
CA346756091
NM_000179.3:c.2896A>T
CA346756094
NM_000179.3:c.2897C>G