Canonical Allele Identifier: PA2826631379
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 922979
ClinVar RCV Id: RCV001183359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu441Phe
CA346752492
NM_001281493.2:c.1323G>T
CA346752494
NM_001281493.2:c.1323G>C