Canonical Allele Identifier: PA2826587322
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234450
ClinVar RCV Id: RCV000216522 RCV000567812 RCV000630217 RCV001201279 RCV003998616 RCV003463610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn1025His
CA072425
NM_001281494.2:c.3073A>C