Canonical Allele Identifier: PA2826626707
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1389492
ClinVar RCV Id: RCV001917373 RCV003365507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp537Val
CA346750663
NM_001281492.2:c.1610A>T