Canonical Allele Identifier: PA2826628825
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188261
ClinVar RCV Id: RCV001020953 RCV001373676 RCV003995614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1107Asp
CA013945
NM_001281492.2:c.3321G>C
CA346761001
NM_001281492.2:c.3321G>T