Canonical Allele Identifier: PA916011644
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182617
ClinVar RCV Id: RCV000160662 RCV001082336 RCV000656893 RCV000780471 RCV000986713 RCV003323296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val50Ile
CA007915
NM_001281494.2:c.148G>A