Canonical Allele Identifier: PA2825112227
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137558
ClinVar RCV Id: RCV003062619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1090Val
CA036542
NM_000257.4:c.3268C>G