Canonical Allele Identifier: PA2825092267
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824176
ClinVar RCV Id: RCV001021079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp1255Asn
CA346761109
NM_000179.3:c.3763G>A