Canonical Allele Identifier: PA2825113056
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3075186
ClinVar RCV Id: RCV004015712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1593Leu
CA389037652
NM_000257.4:c.4777G>T
CA389037653
NM_000257.4:c.4777G>C