Canonical Allele Identifier: PA2826625282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141751
ClinVar RCV Id: RCV000130382 RCV000212639 RCV000475028 RCV000986711 RCV003460924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr203Ile
CA016780
NM_001281492.2:c.608C>T