Canonical Allele Identifier: PA2826632068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410472
ClinVar RCV Id: RCV002230116 RCV004022785
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro601Leu
CA16610917
NM_001281493.2:c.1802C>T