Canonical Allele Identifier: PA658680605
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455138
ClinVar RCV Id: RCV000554233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln485Pro
CA346745731
NM_000179.3:c.1454A>C