Allele Registry

Canonical Allele Identifier: PA094958

Gene: ECM1 HGNC NCBI

ClinVar RCV:

RCV000007902

ClinVar Variation:

7476

HGVS (amino-acid)	Matching Registered Transcripts
NP_004416.2:p.Phe167Ile	CA118819 NM_004425.4:c.499T>A