Canonical Allele Identifier: PA299495
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182651
ClinVar RCV Id: RCV000160704 RCV000168081 RCV000212694 RCV000662520 RCV003330517 RCV003998507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1356Phe
CA015417
NM_000179.3:c.4068G>C
CA346761749
NM_000179.3:c.4068G>T