Canonical Allele Identifier: PA916012246
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185667
ClinVar RCV Id: RCV000165125 RCV000459296 RCV001527033 RCV003995394
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala959Val
CA014254
NM_001281494.2:c.2876C>T