Canonical Allele Identifier: PA916010973
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479864
ClinVar RCV Id: RCV000573137 RCV000707589 RCV001175449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro38Leu
CA346734858
NM_001281492.2:c.113C>T