Canonical Allele Identifier: PA2826635459
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 922889
ClinVar RCV Id: RCV001183196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu336Arg
CA346750209
NM_001281494.2:c.1007T>G