Canonical Allele Identifier: PA2499229401
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007727
ClinVar RCV Id: RCV001304954 RCV003166727
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met799Leu
CA346753874
NM_000179.3:c.2395A>C
CA346753879
NM_000179.3:c.2395A>T