Canonical Allele Identifier: PA2825092561
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719022
ClinVar RCV Id: RCV002296774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1294Ser
CA346761374
NM_000179.3:c.3880T>A
CA346761378
NM_000179.3:c.3881G>C