Canonical Allele Identifier: PA2826587271
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419537
ClinVar RCV Id: RCV000480936 RCV000574295 RCV001348367 RCV004002305
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met1024Thr
CA072409
NM_001281494.2:c.3071T>C