Canonical Allele Identifier: PA2826631224
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89254
ClinVar RCV Id: RCV000074718 RCV001530136 RCV003137606 RCV001854277 RCV003584540
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe404Ser
CA009702
NM_001281493.2:c.1211T>C