Canonical Allele Identifier: PA645378046
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428380
ClinVar RCV Id: RCV000490967 RCV000549468 RCV000759128 RCV004003459 RCV003464056 RCV004535548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr6Pro
CA068021
NM_000179.3:c.16A>C