Canonical Allele Identifier: PA2826631180
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928260
ClinVar RCV Id: RCV001192034 RCV003462666 RCV004010566
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu393Val
CA346750829
NM_001281493.2:c.1177C>G