Canonical Allele Identifier: PA2826635648
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485871
ClinVar RCV Id: RCV000564526 RCV001070185
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu379Phe
CA346750745
NM_001281494.2:c.1135C>T