Canonical Allele Identifier: PA2826633582
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127589
ClinVar RCV Id: RCV000115419 RCV000122966 RCV000212687 RCV001005027 RCV000588959 RCV000659895 RCV001081954 RCV001358662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr941Ser
CA014099
NM_001281493.2:c.2821A>T