Canonical Allele Identifier: PA1139674706
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 922979
ClinVar RCV Id: RCV001183359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu743Phe
CA346752492
NM_000179.3:c.2229G>T
CA346752494
NM_000179.3:c.2229G>C