Canonical Allele Identifier: PA2826627335
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 927353
ClinVar RCV Id: RCV001238343 RCV001190576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu685Phe
CA069075
NM_001281492.2:c.2053C>T