Canonical Allele Identifier: PA916012167
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428304
ClinVar RCV Id: RCV000491347 RCV000502171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu932_Leu933dup
CA645369302
NM_001281494.2:c.2795_2800dup