Canonical Allele Identifier: PA2826629598
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89575
ClinVar RCV Id: RCV001019736
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala24Val
CA016705
NM_001281493.2:c.71C>T