Canonical Allele Identifier: PA191906
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89461
ClinVar RCV Id: RCV000164843 RCV000485038 RCV000559935 RCV000659897 RCV003235031 RCV003460692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg1263Cys
CA014275
NM_000179.3:c.3787C>T