Canonical Allele Identifier: PA2825112817
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072210
ClinVar RCV Id: RCV004012240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1458His
CA389038831
NM_000257.4:c.4374G>T
CA389038834
NM_000257.4:c.4374G>C