Canonical Allele Identifier: PA2826629398
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 824523
ClinVar RCV Id: RCV001021715 RCV001060015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1214Asn
CA346761677
NM_001281492.2:c.3641C>A