Canonical Allele Identifier: PA2826625880
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1042990
ClinVar RCV Id: RCV001347034 RCV003322885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly347Ala
CA346745487
NM_001281492.2:c.1040G>C