Canonical Allele Identifier: PA347267
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 190407
ClinVar RCV Id: RCV000551132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1603Pro
CA347265
NM_000257.4:c.4807G>C