Canonical Allele Identifier: PA913194164
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 626820
ClinVar RCV Id: RCV000770490 RCV001069425 RCV002477754
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn911Tyr
CA389047241
NM_000257.4:c.2731A>T