Canonical Allele Identifier: PA915956561
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 689573
ClinVar RCV Id: RCV000850326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro225Leu
CA389052279
NM_000257.4:c.674C>T