Canonical Allele Identifier: PA916010906
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 632905
ClinVar RCV Id: RCV000780472 RCV001856186 RCV002458395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro12Leu
CA46687631
NM_001281492.2:c.35C>T