Canonical Allele Identifier: PA2826625332
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 187718
ClinVar RCV Id: RCV000167468 RCV000229553 RCV000454816 RCV000524097 RCV000657019 RCV000662908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser216Phe
CA007847
NM_001281492.2:c.647C>T