Canonical Allele Identifier: PA2826630265
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 645807
ClinVar RCV Id: RCV000799965 RCV002388470 RCV004001631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr184Ile
CA067675
NM_001281493.2:c.551C>T