Canonical Allele Identifier: PA357813
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 224584
ClinVar RCV Id: RCV000210179 RCV000791386 RCV001022587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro15Leu
CA357811
NM_000179.3:c.44C>T