Canonical Allele Identifier: PA2826631147
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455175
ClinVar RCV Id: RCV000536294 RCV000776692 RCV004003670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Cys385Ser
CA346750771
NM_001281493.2:c.1153T>A
CA346750775
NM_001281493.2:c.1154G>C