Canonical Allele Identifier: PA916012337
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410530
ClinVar RCV Id: RCV000461225 RCV000574392 RCV000485186 RCV001731697 RCV003483628 RCV004001859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile981dup
CA072217
NM_001281494.2:c.2942_2944dup