Canonical Allele Identifier: PA163997
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140947
ClinVar RCV Id: RCV000129223 RCV000204246 RCV001775618 RCV003997487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1354Pro
CA015365
NM_000179.3:c.4061T>C