Canonical Allele Identifier: PA645414688
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 228919
ClinVar RCV Id: RCV000214819 RCV000796059 RCV002363075 RCV002274965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala229Val
CA10576962
NM_000257.4:c.686C>T