Canonical Allele Identifier: PA916010938
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89562
ClinVar RCV Id: RCV000075031 RCV000115442 RCV000417385 RCV000524214 RCV000765674 RCV001082180 RCV004528274 RCV003482130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala25Ser
CA016371
NM_001281492.2:c.73G>T