Canonical Allele Identifier: PA2573164082
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373197
ClinVar RCV Id: RCV001875070
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu230Ala
CA346739922
NM_000179.3:c.689A>C