Canonical Allele Identifier: PA2826635462
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2741883
ClinVar RCV Id: RCV003593519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu337Gln
CA346750219
NM_001281494.2:c.1009G>C