Canonical Allele Identifier: PA915956567
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 644163
ClinVar RCV Id: RCV000798023
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala233Thr
CA389052235
NM_000257.4:c.697G>A