Canonical Allele Identifier: PA2826626645
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491889
ClinVar RCV Id: RCV000581390 RCV001860090 RCV004002345 RCV004530630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met524Thr
CA068326
NM_001281492.2:c.1571T>C