Canonical Allele Identifier: PA2499230374
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1285419
ClinVar RCV Id: RCV001706775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val191Ile
CA389052511
NM_000257.4:c.571G>A