Canonical Allele Identifier: PA2826630994
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491889
ClinVar RCV Id: RCV000581390 RCV001860090 RCV004002345 RCV004530630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met352Thr
CA068326
NM_001281493.2:c.1055T>C