Canonical Allele Identifier: PA098897
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 195720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1019Asn
CA013337
NM_000257.4:c.3056C>A