Canonical Allele Identifier: PA2826626735
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 422162
ClinVar RCV Id: RCV000480051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly544Val
CA16617664
NM_001281492.2:c.1631G>T