Canonical Allele Identifier: PA2826625186
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182614
ClinVar RCV Id: RCV000160659 RCV001019185 RCV002515116 RCV002247556
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys181Asn
CA016664
NM_001281492.2:c.543A>T
CA346740759
NM_001281492.2:c.543A>C