Canonical Allele Identifier: PA198999
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2442851
ClinVar RCV Id: RCV003150657
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1673Phe
CA015565
NM_000257.4:c.5017A>T