Canonical Allele Identifier: PA2826635646
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076141
ClinVar RCV Id: RCV004018458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu379Pro
CA346750747
NM_001281494.2:c.1136T>C