Canonical Allele Identifier: PA2573177663
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484465
ClinVar RCV Id: RCV002005815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.His970Arg
CA374111825
NM_001083607.3:c.2909A>G