Canonical Allele Identifier: PA2826624943
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 838310
ClinVar RCV Id: RCV001039832 RCV001759737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser124Cys
CA346740166
NM_001281492.2:c.371C>G