Canonical Allele Identifier: PA2826635390
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233917
ClinVar RCV Id: RCV000217487 RCV000464191 RCV000480702 RCV001293521 RCV003998588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly322Val
CA068227
NM_001281494.2:c.965G>T