Canonical Allele Identifier: PA2826626658
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479971
ClinVar RCV Id: RCV000574848 RCV001227127 RCV003492101 RCV004000888
ClinVar Variation Id: 2837716
ClinVar RCV Id: RCV003758378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln527His
CA346750604
NM_001281492.2:c.1581G>C
CA346750605
NM_001281492.2:c.1581G>T