Canonical Allele Identifier: PA2826632347
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234622
ClinVar RCV Id: RCV000218181 RCV000491101 RCV000458194 RCV000623975 RCV003463615 RCV002467444 RCV003165582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr667Cys
CA069803
NM_001281493.2:c.2000A>G