Canonical Allele Identifier: PA916010920
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479878
ClinVar RCV Id: RCV000563575 RCV001218497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala16Val
CA073037
NM_001281492.2:c.47C>T