Canonical Allele Identifier: PA2826625496
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89176
ClinVar RCV Id: RCV000162700 RCV000213163 RCV000411429 RCV000627690 RCV001255541 RCV003460658 RCV003997063
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His252Tyr
CA008133
NM_001281492.2:c.754C>T