Canonical Allele Identifier: PA645384326
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 425199
ClinVar RCV Id: RCV000487547 RCV000775956 RCV003758794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1205Ala
CA16621748
NM_000179.3:c.3613A>G