Canonical Allele Identifier: PA2826633901
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2128264
ClinVar RCV Id: RCV003057495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu1003Ile
CA346761444
NM_001281493.2:c.3007C>A