Canonical Allele Identifier: PA658680154
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455296
ClinVar RCV Id: RCV000551898 RCV000776879 RCV003153678 RCV003226937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg128Cys
CA346737052
NM_000179.3:c.382C>T