Canonical Allele Identifier: PA2826630331
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 946259
ClinVar RCV Id: RCV001217088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser201Pro
CA346746257
NM_001281493.2:c.601T>C