Canonical Allele Identifier: PA2826631351
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188107
ClinVar RCV Id: RCV000167959 RCV000409734 RCV000491880 RCV000759851 RCV003468820 RCV003995600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu433Ile
CA009870
NM_001281493.2:c.1297C>A