Canonical Allele Identifier: PA2826628469
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127587
ClinVar RCV Id: RCV000115416 RCV000212684 RCV000819197 RCV003453035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1032Asp
CA013090
NM_001281492.2:c.3095C>A