Canonical Allele Identifier: PA2826636186
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89283
ClinVar RCV Id: RCV001198423 RCV001293869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val507del
CA010243
NM_001281494.2:c.1520_1522del