Canonical Allele Identifier: PA151470
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89551
ClinVar RCV Id: RCV000075020 RCV000115439 RCV000200987 RCV000586585 RCV001083284 RCV000986708 RCV003492404 RCV002498360 RCV004537284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu220Asp
CA016176
NM_000179.3:c.660A>C
CA346739358
NM_000179.3:c.660A>T