Canonical Allele Identifier: PA184090
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179272
ClinVar RCV Id: RCV000156061 RCV000850503 RCV001727606
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala381Thr
CA010273
NM_000257.4:c.1141G>A