Canonical Allele Identifier: PA2826631095
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682021
ClinVar RCV Id: RCV003477313 RCV003594701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys374Ile
CA346750714
NM_001281493.2:c.1121A>T