Canonical Allele Identifier: PA645382295
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237160
ClinVar RCV Id: RCV001372750
ClinVar Variation Id: 336443
ClinVar RCV Id: RCV000276074 RCV000630372 RCV002256216 RCV003463784
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys854Asn
CA069186
NM_000179.3:c.2562G>T
CA10582064
NM_000179.3:c.2562G>C