Canonical Allele Identifier: PA2826629302
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419537
ClinVar RCV Id: RCV000480936 RCV000574295 RCV001348367 RCV004002305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met1196Thr
CA072409
NM_001281492.2:c.3587T>C