Canonical Allele Identifier: PA2573192720
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470503
ClinVar RCV Id: RCV001995237
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu909Phe
CA346760606
NM_001281494.2:c.2725C>T