Canonical Allele Identifier: PA357826
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224580
ClinVar RCV Id: RCV000210205 RCV000410099 RCV000524121 RCV000575424 RCV001284178 RCV003479062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser616Cys
CA068191
NM_000179.3:c.1847C>G