Canonical Allele Identifier: PA338297
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216295
ClinVar RCV Id: RCV000198916 RCV000570887 RCV003996992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Pro44Leu
CA338295
NM_000179.3:c.131C>T