Canonical Allele Identifier: PA164526
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141122
ClinVar RCV Id: RCV000129487 RCV000168210 RCV000216085 RCV000589579 RCV000662957 RCV000708859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg302Thr
CA016638
NM_000179.3:c.905G>C