Canonical Allele Identifier: PA2826629241
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801224
ClinVar RCV Id: RCV000985849 RCV003594065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His1187Tyr
CA346761520
NM_001281492.2:c.3559C>T