Canonical Allele Identifier: PA2826632890
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 654260
ClinVar RCV Id: RCV000810186
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys790Asn
CA346758280
NM_001281493.2:c.2370A>C
CA346758284
NM_001281493.2:c.2370A>T