Canonical Allele Identifier: PA2573165091
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1481864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser948Leu
CA389046849
NM_000257.4:c.2843C>T