Canonical Allele Identifier: PA913194020
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 635223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg249Leu
CA389052134
NM_000257.4:c.746G>T