Canonical Allele Identifier: PA2826627133
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419197
ClinVar RCV Id: RCV000542142 RCV000662407 RCV000580933 RCV000765686 RCV001284514 RCV004002290
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr637Ser
CA068780
NM_001281492.2:c.1909A>T
CA068793
NM_001281492.2:c.1910C>G