Canonical Allele Identifier: PA299431
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182621
ClinVar RCV Id: RCV000160666 RCV000195871 RCV000563544 RCV000780479 RCV003998492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser405Cys
CA008320
NM_000179.3:c.1214C>G