Canonical Allele Identifier: PA2826633383
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89423
ClinVar RCV Id: RCV000220560 RCV000483164 RCV000684810 RCV000767044 RCV003466949
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu899Val
CA013502
NM_001281493.2:c.2695C>G