Canonical Allele Identifier: PA2825091881
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733005
ClinVar RCV Id: RCV002455140 RCV003594199
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1198Val
CA346760541
NM_000179.3:c.3593C>T