Canonical Allele Identifier: PA2826636227
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 952383
ClinVar RCV Id: RCV001224487 RCV002447127
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu516Ile
CA346754072
NM_001281494.2:c.1546C>A