Canonical Allele Identifier: PA2573166287
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395941
ClinVar RCV Id: RCV001891512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp239Ala
CA389052201
NM_000257.4:c.716A>C