Canonical Allele Identifier: PA916011398
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 420757
ClinVar RCV Id: RCV000484206 RCV001019455 RCV001303106 RCV004003333
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr955Ile
CA16617694
NM_001281492.2:c.2864C>T