Canonical Allele Identifier: PA891846335
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 583061
ClinVar RCV Id: RCV000707298 RCV001020752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1209Val
CA346760595
NM_000179.3:c.3625C>G