Canonical Allele Identifier: PA2826632834
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842837
ClinVar RCV Id: RCV001045322 RCV001183346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro780Gln
CA346758111
NM_001281493.2:c.2339C>A