Canonical Allele Identifier: PA2826631683
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 927353
ClinVar RCV Id: RCV001238343 RCV001190576
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu513Phe
CA069075
NM_001281493.2:c.1537C>T