Canonical Allele Identifier: PA2826631466
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444
ClinVar RCV Id: RCV000163700 RCV000480884 RCV000630065 RCV000662379 RCV002307420 RCV003462122 RCV003995273
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr462Asn
CA009966
NM_001281493.2:c.1385C>A