Canonical Allele Identifier: PA296779
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181318
ClinVar RCV Id: RCV000158755 RCV003586157
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala233Ser
CA016631
NM_000257.4:c.697G>T