Canonical Allele Identifier: PA2826636265
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455201
ClinVar RCV Id: RCV000541502 RCV001178553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn525del
CA658655816
NM_001281494.2:c.1573_1575del