Canonical Allele Identifier: PA261354
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu915Pro
CA013003
NM_000257.4:c.2744T>C