Canonical Allele Identifier: PA2826631693
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791477
ClinVar RCV Id: RCV002450508
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp515Val
CA346754067
NM_001281493.2:c.1544A>T