Canonical Allele Identifier: PA658802520
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525810
ClinVar RCV Id: RCV000630131 RCV002457990 RCV004002792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser1195Thr
CA071428
NM_000179.3:c.3584G>C