Canonical Allele Identifier: PA2826635598
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784363
ClinVar RCV Id: RCV002417300 RCV003464541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly368Trp
CA346750678
NM_001281494.2:c.1102G>T