Canonical Allele Identifier: PA658744313
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491990
ClinVar RCV Id: RCV000584251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr235Ile
CA346739977
NM_000179.3:c.704C>T