Canonical Allele Identifier: PA1139674931
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845264
ClinVar RCV Id: RCV001048297
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr767_Pro768del
CA916079957
NM_000179.3:c.2299_2304del