Canonical Allele Identifier: PA916010875
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232954
ClinVar RCV Id: RCV000219646 RCV000485238 RCV000793054 RCV000680209
ClinVar Variation Id: 483877
ClinVar RCV Id: RCV000569131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1Ile