Canonical Allele Identifier: PA2826636011
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 141058
ClinVar RCV Id: RCV000129397 RCV000410431 RCV000477388 RCV000501569 RCV000622945 RCV001353758 RCV001257543 RCV001251301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr465Ile
CA009983
NM_001281494.2:c.1394C>T