Canonical Allele Identifier: PA2826634861
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 946259
ClinVar RCV Id: RCV001217088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser201Pro
CA346746257
NM_001281494.2:c.601T>C