Canonical Allele Identifier: PA2826631142
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410509
ClinVar RCV Id: RCV000460149 RCV000775722 RCV001576673 RCV001797726 RCV004001851
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly384Cys
CA16610900
NM_001281493.2:c.1150G>T